Canonical Allele Identifier: CA343773552
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2777316
ClinVar RCV Id: RCV003638990
MyVariant Identifiers: chr1:g.173878733C>T (hg19) chr1:g.173909595C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909595C>T , CM000663.2:g.173909595C>T GRCh38
NC_000001.10:g.173878733C>T , CM000663.1:g.173878733C>T GRCh37
NC_000001.9:g.172145356C>T NCBI36
NG_012462.1:g.12784G>A , LRG_577:g.12784G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1110G>A MANE Select ENSP00000356671.3:p.Met370Ile
ENST00000367698.3:c.1110G>A ENSP00000356671.3:p.Met370Ile
ENST00000617423.4:c.560-2102G>A ENSP00000478688.1:n.560-2102G>A
NM_000488.3:c.1110G>A , LRG_577t1:c.1110G>A NP_000479.1:p.Met370Ile
XM_005245198.2:c.966G>A XP_005245255.1:p.Met322Ile
NM_001365052.1:c.966G>A NP_001351981.1:p.Met322Ile
NM_000488.4:c.1110G>A MANE Select NP_000479.1:p.Met370Ile
NM_001365052.2:c.966G>A NP_001351981.1:p.Met322Ile
NM_001386302.1:c.1233G>A NP_001373231.1:p.Met411Ile
NM_001386303.1:c.1191G>A NP_001373232.1:p.Met397Ile
NM_001386304.1:c.1089G>A NP_001373233.1:p.Met363Ile
NM_001386305.1:c.1053G>A NP_001373234.1:p.Met351Ile
NM_001386306.1:c.894G>A NP_001373235.1:p.Met298Ile
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