Canonical Allele Identifier: CA343773668
Gene: SERPINC1 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1057C>G MANE Select ENSP00000356671.3:p.Pro353Ala
ENST00000367698.3:c.1057C>G ENSP00000356671.3:p.Pro353Ala
ENST00000617423.4:c.560-2155C>G ENSP00000478688.1:n.560-2155C>G
NM_000488.3:c.1057C>G , LRG_577t1:c.1057C>G NP_000479.1:p.Pro353Ala
XM_005245198.2:c.913C>G XP_005245255.1:p.Pro305Ala
NM_001365052.1:c.913C>G NP_001351981.1:p.Pro305Ala
NM_000488.4:c.1057C>G MANE Select NP_000479.1:p.Pro353Ala
NM_001365052.2:c.913C>G NP_001351981.1:p.Pro305Ala
NM_001386302.1:c.1180C>G NP_001373231.1:p.Pro394Ala
NM_001386303.1:c.1138C>G NP_001373232.1:p.Pro380Ala
NM_001386304.1:c.1036C>G NP_001373233.1:p.Pro346Ala
NM_001386305.1:c.1000C>G NP_001373234.1:p.Pro334Ala
NM_001386306.1:c.841C>G NP_001373235.1:p.Pro281Ala
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