Canonical Allele Identifier: CA421823382

Gene: SERPINC1

Linked Data

• gnomAD v4: 1-173914589-C-A
• MyVariant Identifiers: chr1:g.173883727C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173914589C>A , CM000663.2:g.173914589C>A	GRCh38
NC_000001.10:g.173883727C>A , CM000663.1:g.173883727C>A	GRCh37
NC_000001.9:g.172150350C>A	NCBI36
NG_012462.1:g.7790G>T , LRG_577:g.7790G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.372G>T MANE Select	ENSP00000356671.3:p.Leu124=
ENST00000367698.3:c.372G>T	ENSP00000356671.3:p.Leu124=
ENST00000487183.1:n.77G>T
ENST00000494024.1:n.598G>T
ENST00000617423.4:c.372G>T	ENSP00000478688.1:p.Leu124=
NM_000488.3:c.372G>T , LRG_577t1:c.372G>T	NP_000479.1:p.Leu124=
XM_005245198.2:c.228G>T	XP_005245255.1:p.Leu76=
NM_001365052.1:c.228G>T	NP_001351981.1:p.Leu76=
NM_000488.4:c.372G>T MANE Select	NP_000479.1:p.Leu124=
NM_001365052.2:c.228G>T	NP_001351981.1:p.Leu76=
NM_001386302.1:c.372G>T	NP_001373231.1:p.Leu124=
NM_001386303.1:c.453G>T	NP_001373232.1:p.Leu151=
NM_001386304.1:c.372G>T	NP_001373233.1:p.Leu124=
NM_001386305.1:c.372G>T	NP_001373234.1:p.Leu124=
NM_001386306.1:c.372G>T	NP_001373235.1:p.Leu124=