Canonical Allele Identifier: CA343776668

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173881082C>A (hg19) ; chr1:g.173911944C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911944C>A , CM000663.2:g.173911944C>A	GRCh38
NC_000001.10:g.173881082C>A , CM000663.1:g.173881082C>A	GRCh37
NC_000001.9:g.172147705C>A	NCBI36
NG_012462.1:g.10435G>T , LRG_577:g.10435G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.479G>T MANE Select	ENSP00000356671.3:p.Cys160Phe
ENST00000367698.3:c.479G>T	ENSP00000356671.3:p.Cys160Phe
ENST00000487183.1:n.184G>T
ENST00000617423.4:c.479G>T	ENSP00000478688.1:p.Cys160Phe
NM_000488.3:c.479G>T , LRG_577t1:c.479G>T	NP_000479.1:p.Cys160Phe
XM_005245198.2:c.335G>T	XP_005245255.1:p.Cys112Phe
NM_001365052.1:c.335G>T	NP_001351981.1:p.Cys112Phe
NM_000488.4:c.479G>T MANE Select	NP_000479.1:p.Cys160Phe
NM_001365052.2:c.335G>T	NP_001351981.1:p.Cys112Phe
NM_001386302.1:c.479G>T	NP_001373231.1:p.Cys160Phe
NM_001386303.1:c.560G>T	NP_001373232.1:p.Cys187Phe
NM_001386304.1:c.479G>T	NP_001373233.1:p.Cys160Phe
NM_001386305.1:c.479G>T	NP_001373234.1:p.Cys160Phe
NM_001386306.1:c.409-1053G>T	NP_001373235.1:n.409-1053G>T