Canonical Allele Identifier: CA421942991

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878883A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909745A>T , CM000663.2:g.173909745A>T	GRCh38
NC_000001.10:g.173878883A>T , CM000663.1:g.173878883A>T	GRCh37
NC_000001.9:g.172145506A>T	NCBI36
NG_012462.1:g.12634T>A , LRG_577:g.12634T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.960T>A MANE Select	ENSP00000356671.3:p.Pro320=
ENST00000367698.3:c.960T>A	ENSP00000356671.3:p.Pro320=
ENST00000487183.1:n.611T>A
ENST00000617423.4:c.559+2119T>A	ENSP00000478688.1:n.559+2119T>A
NM_000488.3:c.960T>A , LRG_577t1:c.960T>A	NP_000479.1:p.Pro320=
XM_005245198.2:c.816T>A	XP_005245255.1:p.Pro272=
NM_001365052.1:c.816T>A	NP_001351981.1:p.Pro272=
NM_000488.4:c.960T>A MANE Select	NP_000479.1:p.Pro320=
NM_001365052.2:c.816T>A	NP_001351981.1:p.Pro272=
NM_001386302.1:c.1083T>A	NP_001373231.1:p.Pro361=
NM_001386303.1:c.1041T>A	NP_001373232.1:p.Pro347=
NM_001386304.1:c.939T>A	NP_001373233.1:p.Pro313=
NM_001386305.1:c.903T>A	NP_001373234.1:p.Pro301=
NM_001386306.1:c.744T>A	NP_001373235.1:p.Pro248=