Canonical Allele Identifier: CA32780206

Gene: SERPINC1

Linked Data

• dbSNP Id: rs909946904
• MyVariant Identifiers: chr1:g.173878709A>C (hg19) ; chr1:g.173909571A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909571A>C , CM000663.2:g.173909571A>C	GRCh38
NC_000001.10:g.173878709A>C , CM000663.1:g.173878709A>C	GRCh37
NC_000001.9:g.172145332A>C	NCBI36
NG_012462.1:g.12808T>G , LRG_577:g.12808T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1134T>G MANE Select	ENSP00000356671.3:p.Pro378=
ENST00000367698.3:c.1134T>G	ENSP00000356671.3:p.Pro378=
ENST00000617423.4:c.560-2078T>G	ENSP00000478688.1:n.560-2078T>G
NM_000488.3:c.1134T>G , LRG_577t1:c.1134T>G	NP_000479.1:p.Pro378=
XM_005245198.2:c.990T>G	XP_005245255.1:p.Pro330=
NM_001365052.1:c.990T>G	NP_001351981.1:p.Pro330=
NM_000488.4:c.1134T>G MANE Select	NP_000479.1:p.Pro378=
NM_001365052.2:c.990T>G	NP_001351981.1:p.Pro330=
NM_001386302.1:c.1257T>G	NP_001373231.1:p.Pro419=
NM_001386303.1:c.1215T>G	NP_001373232.1:p.Pro405=
NM_001386304.1:c.1113T>G	NP_001373233.1:p.Pro371=
NM_001386305.1:c.1077T>G	NP_001373234.1:p.Pro359=
NM_001386306.1:c.918T>G	NP_001373235.1:p.Pro306=