Canonical Allele Identifier: CA343777709

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173883828C>T (hg19) ; chr1:g.173914690C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914690C>T , CM000663.2:g.173914690C>T	GRCh38
NC_000001.10:g.173883828C>T , CM000663.1:g.173883828C>T	GRCh37
NC_000001.9:g.172150451C>T	NCBI36
NG_012462.1:g.7689G>A , LRG_577:g.7689G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.271G>A MANE Select	ENSP00000356671.3:p.Ala91Thr
ENST00000367698.3:c.271G>A	ENSP00000356671.3:p.Ala91Thr
ENST00000494024.1:n.497G>A
ENST00000617423.4:c.271G>A	ENSP00000478688.1:p.Ala91Thr
NM_000488.3:c.271G>A , LRG_577t1:c.271G>A	NP_000479.1:p.Ala91Thr
XM_005245198.2:c.127G>A	XP_005245255.1:p.Ala43Thr
NM_001365052.1:c.127G>A	NP_001351981.1:p.Ala43Thr
NM_000488.4:c.271G>A MANE Select	NP_000479.1:p.Ala91Thr
NM_001365052.2:c.127G>A	NP_001351981.1:p.Ala43Thr
NM_001386302.1:c.271G>A	NP_001373231.1:p.Ala91Thr
NM_001386303.1:c.352G>A	NP_001373232.1:p.Ala118Thr
NM_001386304.1:c.271G>A	NP_001373233.1:p.Ala91Thr
NM_001386305.1:c.271G>A	NP_001373234.1:p.Ala91Thr
NM_001386306.1:c.271G>A	NP_001373235.1:p.Ala91Thr