Canonical Allele Identifier: CA343773622

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878762A>T (hg19) ; chr1:g.173909624A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909624A>T , CM000663.2:g.173909624A>T	GRCh38
NC_000001.10:g.173878762A>T , CM000663.1:g.173878762A>T	GRCh37
NC_000001.9:g.172145385A>T	NCBI36
NG_012462.1:g.12755T>A , LRG_577:g.12755T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1081T>A MANE Select	ENSP00000356671.3:p.Phe361Ile
ENST00000367698.3:c.1081T>A	ENSP00000356671.3:p.Phe361Ile
ENST00000617423.4:c.560-2131T>A	ENSP00000478688.1:n.560-2131T>A
NM_000488.3:c.1081T>A , LRG_577t1:c.1081T>A	NP_000479.1:p.Phe361Ile
XM_005245198.2:c.937T>A	XP_005245255.1:p.Phe313Ile
NM_001365052.1:c.937T>A	NP_001351981.1:p.Phe313Ile
NM_000488.4:c.1081T>A MANE Select	NP_000479.1:p.Phe361Ile
NM_001365052.2:c.937T>A	NP_001351981.1:p.Phe313Ile
NM_001386302.1:c.1204T>A	NP_001373231.1:p.Phe402Ile
NM_001386303.1:c.1162T>A	NP_001373232.1:p.Phe388Ile
NM_001386304.1:c.1060T>A	NP_001373233.1:p.Phe354Ile
NM_001386305.1:c.1024T>A	NP_001373234.1:p.Phe342Ile
NM_001386306.1:c.865T>A	NP_001373235.1:p.Phe289Ile