Canonical Allele Identifier: CA421822958

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173880961G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911823G>T , CM000663.2:g.173911823G>T	GRCh38
NC_000001.10:g.173880961G>T , CM000663.1:g.173880961G>T	GRCh37
NC_000001.9:g.172147584G>T	NCBI36
NG_012462.1:g.10556C>A , LRG_577:g.10556C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.600C>A MANE Select	ENSP00000356671.3:p.Ala200=
ENST00000367698.3:c.600C>A	ENSP00000356671.3:p.Ala200=
ENST00000487183.1:n.305C>A
ENST00000617423.4:c.559+41C>A	ENSP00000478688.1:n.559+41C>A
NM_000488.3:c.600C>A , LRG_577t1:c.600C>A	NP_000479.1:p.Ala200=
XM_005245198.2:c.456C>A	XP_005245255.1:p.Ala152=
NM_001365052.1:c.456C>A	NP_001351981.1:p.Ala152=
NM_000488.4:c.600C>A MANE Select	NP_000479.1:p.Ala200=
NM_001365052.2:c.456C>A	NP_001351981.1:p.Ala152=
NM_001386302.1:c.600C>A	NP_001373231.1:p.Ala200=
NM_001386303.1:c.681C>A	NP_001373232.1:p.Ala227=
NM_001386304.1:c.600C>A	NP_001373233.1:p.Ala200=
NM_001386305.1:c.600C>A	NP_001373234.1:p.Ala200=
NM_001386306.1:c.409-932C>A	NP_001373235.1:n.409-932C>A