Canonical Allele Identifier: CA343774753

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173879049T>A (hg19) ; chr1:g.173909911T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909911T>A , CM000663.2:g.173909911T>A	GRCh38
NC_000001.10:g.173879049T>A , CM000663.1:g.173879049T>A	GRCh37
NC_000001.9:g.172145672T>A	NCBI36
NG_012462.1:g.12468A>T , LRG_577:g.12468A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.794A>T MANE Select	ENSP00000356671.3:p.Asn265Ile
ENST00000367698.3:c.794A>T	ENSP00000356671.3:p.Asn265Ile
ENST00000487183.1:n.445A>T
ENST00000617423.4:c.559+1953A>T	ENSP00000478688.1:n.559+1953A>T
NM_000488.3:c.794A>T , LRG_577t1:c.794A>T	NP_000479.1:p.Asn265Ile
XM_005245198.2:c.650A>T	XP_005245255.1:p.Asn217Ile
NM_001365052.1:c.650A>T	NP_001351981.1:p.Asn217Ile
NM_000488.4:c.794A>T MANE Select	NP_000479.1:p.Asn265Ile
NM_001365052.2:c.650A>T	NP_001351981.1:p.Asn217Ile
NM_001386302.1:c.917A>T	NP_001373231.1:p.Asn306Ile
NM_001386303.1:c.875A>T	NP_001373232.1:p.Asn292Ile
NM_001386304.1:c.773A>T	NP_001373233.1:p.Asn258Ile
NM_001386305.1:c.763-26A>T	NP_001373234.1:n.763-26A>T
NM_001386306.1:c.578A>T	NP_001373235.1:p.Asn193Ile