Canonical Allele Identifier: CA421942762

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879003T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909865T>G , CM000663.2:g.173909865T>G	GRCh38
NC_000001.10:g.173879003T>G , CM000663.1:g.173879003T>G	GRCh37
NC_000001.9:g.172145626T>G	NCBI36
NG_012462.1:g.12514A>C , LRG_577:g.12514A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.840A>C MANE Select	ENSP00000356671.3:p.Ser280=
ENST00000367698.3:c.840A>C	ENSP00000356671.3:p.Ser280=
ENST00000487183.1:n.491A>C
ENST00000617423.4:c.559+1999A>C	ENSP00000478688.1:n.559+1999A>C
NM_000488.3:c.840A>C , LRG_577t1:c.840A>C	NP_000479.1:p.Ser280=
XM_005245198.2:c.696A>C	XP_005245255.1:p.Ser232=
NM_001365052.1:c.696A>C	NP_001351981.1:p.Ser232=
NM_000488.4:c.840A>C MANE Select	NP_000479.1:p.Ser280=
NM_001365052.2:c.696A>C	NP_001351981.1:p.Ser232=
NM_001386302.1:c.963A>C	NP_001373231.1:p.Ser321=
NM_001386303.1:c.921A>C	NP_001373232.1:p.Ser307=
NM_001386304.1:c.819A>C	NP_001373233.1:p.Ser273=
NM_001386305.1:c.783A>C	NP_001373234.1:p.Ser261=
NM_001386306.1:c.624A>C	NP_001373235.1:p.Ser208=