Canonical Allele Identifier: CA343772629

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873170T>G (hg19) ; chr1:g.173904032T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904032T>G , CM000663.2:g.173904032T>G	GRCh38
NC_000001.10:g.173873170T>G , CM000663.1:g.173873170T>G	GRCh37
NC_000001.9:g.172139793T>G	NCBI36
NG_012462.1:g.18347A>C , LRG_577:g.18347A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1252A>C MANE Select	ENSP00000356671.3:p.Thr418Pro
ENST00000367698.3:c.1252A>C	ENSP00000356671.3:p.Thr418Pro
ENST00000617423.4:c.637A>C	ENSP00000478688.1:p.Thr213Pro
NM_000488.3:c.1252A>C , LRG_577t1:c.1252A>C	NP_000479.1:p.Thr418Pro
XM_005245198.2:c.1108A>C	XP_005245255.1:p.Thr370Pro
NM_001365052.1:c.1108A>C	NP_001351981.1:p.Thr370Pro
NM_000488.4:c.1252A>C MANE Select	NP_000479.1:p.Thr418Pro
NM_001365052.2:c.1108A>C	NP_001351981.1:p.Thr370Pro
NM_001386302.1:c.1375A>C	NP_001373231.1:p.Thr459Pro
NM_001386303.1:c.1333A>C	NP_001373232.1:p.Thr445Pro
NM_001386304.1:c.1231A>C	NP_001373233.1:p.Thr411Pro
NM_001386305.1:c.1195A>C	NP_001373234.1:p.Thr399Pro
NM_001386306.1:c.1036A>C	NP_001373235.1:p.Thr346Pro