Canonical Allele Identifier: CA343772411

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873115G>A (hg19) ; chr1:g.173903977G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903977G>A , CM000663.2:g.173903977G>A	GRCh38
NC_000001.10:g.173873115G>A , CM000663.1:g.173873115G>A	GRCh37
NC_000001.9:g.172139738G>A	NCBI36
NG_012462.1:g.18402C>T , LRG_577:g.18402C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1307C>T MANE Select	ENSP00000356671.3:p.Ala436Val
ENST00000367698.3:c.1307C>T	ENSP00000356671.3:p.Ala436Val
ENST00000617423.4:c.692C>T	ENSP00000478688.1:p.Ala231Val
NM_000488.3:c.1307C>T , LRG_577t1:c.1307C>T	NP_000479.1:p.Ala436Val
XM_005245198.2:c.1163C>T	XP_005245255.1:p.Ala388Val
NM_001365052.1:c.1163C>T	NP_001351981.1:p.Ala388Val
NM_000488.4:c.1307C>T MANE Select	NP_000479.1:p.Ala436Val
NM_001365052.2:c.1163C>T	NP_001351981.1:p.Ala388Val
NM_001386302.1:c.1430C>T	NP_001373231.1:p.Ala477Val
NM_001386303.1:c.1388C>T	NP_001373232.1:p.Ala463Val
NM_001386304.1:c.1286C>T	NP_001373233.1:p.Ala429Val
NM_001386305.1:c.1250C>T	NP_001373234.1:p.Ala417Val
NM_001386306.1:c.1091C>T	NP_001373235.1:p.Ala364Val