Canonical Allele Identifier: CA343772172

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873070G>A (hg19) ; chr1:g.173903932G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903932G>A , CM000663.2:g.173903932G>A	GRCh38
NC_000001.10:g.173873070G>A , CM000663.1:g.173873070G>A	GRCh37
NC_000001.9:g.172139693G>A	NCBI36
NG_012462.1:g.18447C>T , LRG_577:g.18447C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1352C>T MANE Select	ENSP00000356671.3:p.Thr451Ile
ENST00000367698.3:c.1352C>T	ENSP00000356671.3:p.Thr451Ile
ENST00000617423.4:c.737C>T	ENSP00000478688.1:p.Thr246Ile
NM_000488.3:c.1352C>T , LRG_577t1:c.1352C>T	NP_000479.1:p.Thr451Ile
XM_005245198.2:c.1208C>T	XP_005245255.1:p.Thr403Ile
NM_001365052.1:c.1208C>T	NP_001351981.1:p.Thr403Ile
NM_000488.4:c.1352C>T MANE Select	NP_000479.1:p.Thr451Ile
NM_001365052.2:c.1208C>T	NP_001351981.1:p.Thr403Ile
NM_001386302.1:c.1475C>T	NP_001373231.1:p.Thr492Ile
NM_001386303.1:c.1433C>T	NP_001373232.1:p.Thr478Ile
NM_001386304.1:c.1331C>T	NP_001373233.1:p.Thr444Ile
NM_001386305.1:c.1295C>T	NP_001373234.1:p.Thr432Ile
NM_001386306.1:c.1136C>T	NP_001373235.1:p.Thr379Ile