Canonical Allele Identifier: CA343773669
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878786G>T (hg19) chr1:g.173909648G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909648G>T , CM000663.2:g.173909648G>T GRCh38
NC_000001.10:g.173878786G>T , CM000663.1:g.173878786G>T GRCh37
NC_000001.9:g.172145409G>T NCBI36
NG_012462.1:g.12731C>A , LRG_577:g.12731C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1057C>A MANE Select ENSP00000356671.3:p.Pro353Thr
ENST00000367698.3:c.1057C>A ENSP00000356671.3:p.Pro353Thr
ENST00000617423.4:c.560-2155C>A ENSP00000478688.1:n.560-2155C>A
NM_000488.3:c.1057C>A , LRG_577t1:c.1057C>A NP_000479.1:p.Pro353Thr
XM_005245198.2:c.913C>A XP_005245255.1:p.Pro305Thr
NM_001365052.1:c.913C>A NP_001351981.1:p.Pro305Thr
NM_000488.4:c.1057C>A MANE Select NP_000479.1:p.Pro353Thr
NM_001365052.2:c.913C>A NP_001351981.1:p.Pro305Thr
NM_001386302.1:c.1180C>A NP_001373231.1:p.Pro394Thr
NM_001386303.1:c.1138C>A NP_001373232.1:p.Pro380Thr
NM_001386304.1:c.1036C>A NP_001373233.1:p.Pro346Thr
NM_001386305.1:c.1000C>A NP_001373234.1:p.Pro334Thr
NM_001386306.1:c.841C>A NP_001373235.1:p.Pro281Thr
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