Canonical Allele Identifier: CA343774012

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878865C>G (hg19) ; chr1:g.173909727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909727C>G , CM000663.2:g.173909727C>G	GRCh38
NC_000001.10:g.173878865C>G , CM000663.1:g.173878865C>G	GRCh37
NC_000001.9:g.172145488C>G	NCBI36
NG_012462.1:g.12652G>C , LRG_577:g.12652G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.978G>C MANE Select	ENSP00000356671.3:p.Lys326Asn
ENST00000367698.3:c.978G>C	ENSP00000356671.3:p.Lys326Asn
ENST00000617423.4:c.559+2137G>C	ENSP00000478688.1:n.559+2137G>C
NM_000488.3:c.978G>C , LRG_577t1:c.978G>C	NP_000479.1:p.Lys326Asn
XM_005245198.2:c.834G>C	XP_005245255.1:p.Lys278Asn
NM_001365052.1:c.834G>C	NP_001351981.1:p.Lys278Asn
NM_000488.4:c.978G>C MANE Select	NP_000479.1:p.Lys326Asn
NM_001365052.2:c.834G>C	NP_001351981.1:p.Lys278Asn
NM_001386302.1:c.1101G>C	NP_001373231.1:p.Lys367Asn
NM_001386303.1:c.1059G>C	NP_001373232.1:p.Lys353Asn
NM_001386304.1:c.957G>C	NP_001373233.1:p.Lys319Asn
NM_001386305.1:c.921G>C	NP_001373234.1:p.Lys307Asn
NM_001386306.1:c.762G>C	NP_001373235.1:p.Lys254Asn