Canonical Allele Identifier: CA343774779

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879059T>A (hg19) ; chr1:g.173909921T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909921T>A , CM000663.2:g.173909921T>A	GRCh38
NC_000001.10:g.173879059T>A , CM000663.1:g.173879059T>A	GRCh37
NC_000001.9:g.172145682T>A	NCBI36
NG_012462.1:g.12458A>T , LRG_577:g.12458A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.784A>T MANE Select	ENSP00000356671.3:p.Ser262Cys
ENST00000367698.3:c.784A>T	ENSP00000356671.3:p.Ser262Cys
ENST00000487183.1:n.435A>T
ENST00000617423.4:c.559+1943A>T	ENSP00000478688.1:n.559+1943A>T
NM_000488.3:c.784A>T , LRG_577t1:c.784A>T	NP_000479.1:p.Ser262Cys
XM_005245198.2:c.640A>T	XP_005245255.1:p.Ser214Cys
NM_001365052.1:c.640A>T	NP_001351981.1:p.Ser214Cys
NM_000488.4:c.784A>T MANE Select	NP_000479.1:p.Ser262Cys
NM_001365052.2:c.640A>T	NP_001351981.1:p.Ser214Cys
NM_001386302.1:c.907A>T	NP_001373231.1:p.Ser303Cys
NM_001386303.1:c.865A>T	NP_001373232.1:p.Ser289Cys
NM_001386304.1:c.763A>T	NP_001373233.1:p.Ser255Cys
NM_001386305.1:c.763-36A>T	NP_001373234.1:n.763-36A>T
NM_001386306.1:c.568A>T	NP_001373235.1:p.Ser190Cys