Canonical Allele Identifier: CA343772174

Gene: SERPINC1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1352C>A MANE Select	ENSP00000356671.3:p.Thr451Asn
ENST00000367698.3:c.1352C>A	ENSP00000356671.3:p.Thr451Asn
ENST00000617423.4:c.737C>A	ENSP00000478688.1:p.Thr246Asn
NM_000488.3:c.1352C>A , LRG_577t1:c.1352C>A	NP_000479.1:p.Thr451Asn
XM_005245198.2:c.1208C>A	XP_005245255.1:p.Thr403Asn
NM_001365052.1:c.1208C>A	NP_001351981.1:p.Thr403Asn
NM_000488.4:c.1352C>A MANE Select	NP_000479.1:p.Thr451Asn
NM_001365052.2:c.1208C>A	NP_001351981.1:p.Thr403Asn
NM_001386302.1:c.1475C>A	NP_001373231.1:p.Thr492Asn
NM_001386303.1:c.1433C>A	NP_001373232.1:p.Thr478Asn
NM_001386304.1:c.1331C>A	NP_001373233.1:p.Thr444Asn
NM_001386305.1:c.1295C>A	NP_001373234.1:p.Thr432Asn
NM_001386306.1:c.1136C>A	NP_001373235.1:p.Thr379Asn