Canonical Allele Identifier: CA343774504

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878985C>A (hg19) ; chr1:g.173909847C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909847C>A , CM000663.2:g.173909847C>A	GRCh38
NC_000001.10:g.173878985C>A , CM000663.1:g.173878985C>A	GRCh37
NC_000001.9:g.172145608C>A	NCBI36
NG_012462.1:g.12532G>T , LRG_577:g.12532G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.858G>T MANE Select	ENSP00000356671.3:p.Gln286His
ENST00000367698.3:c.858G>T	ENSP00000356671.3:p.Gln286His
ENST00000487183.1:n.509G>T
ENST00000617423.4:c.559+2017G>T	ENSP00000478688.1:n.559+2017G>T
NM_000488.3:c.858G>T , LRG_577t1:c.858G>T	NP_000479.1:p.Gln286His
XM_005245198.2:c.714G>T	XP_005245255.1:p.Gln238His
NM_001365052.1:c.714G>T	NP_001351981.1:p.Gln238His
NM_000488.4:c.858G>T MANE Select	NP_000479.1:p.Gln286His
NM_001365052.2:c.714G>T	NP_001351981.1:p.Gln238His
NM_001386302.1:c.981G>T	NP_001373231.1:p.Gln327His
NM_001386303.1:c.939G>T	NP_001373232.1:p.Gln313His
NM_001386304.1:c.837G>T	NP_001373233.1:p.Gln279His
NM_001386305.1:c.801G>T	NP_001373234.1:p.Gln267His
NM_001386306.1:c.642G>T	NP_001373235.1:p.Gln214His