Canonical Allele Identifier: CA343772475

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173873125T>C (hg19) ; chr1:g.173903987T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903987T>C , CM000663.2:g.173903987T>C	GRCh38
NC_000001.10:g.173873125T>C , CM000663.1:g.173873125T>C	GRCh37
NC_000001.9:g.172139748T>C	NCBI36
NG_012462.1:g.18392A>G , LRG_577:g.18392A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1297A>G MANE Select	ENSP00000356671.3:p.Thr433Ala
ENST00000367698.3:c.1297A>G	ENSP00000356671.3:p.Thr433Ala
ENST00000617423.4:c.682A>G	ENSP00000478688.1:p.Thr228Ala
NM_000488.3:c.1297A>G , LRG_577t1:c.1297A>G	NP_000479.1:p.Thr433Ala
XM_005245198.2:c.1153A>G	XP_005245255.1:p.Thr385Ala
NM_001365052.1:c.1153A>G	NP_001351981.1:p.Thr385Ala
NM_000488.4:c.1297A>G MANE Select	NP_000479.1:p.Thr433Ala
NM_001365052.2:c.1153A>G	NP_001351981.1:p.Thr385Ala
NM_001386302.1:c.1420A>G	NP_001373231.1:p.Thr474Ala
NM_001386303.1:c.1378A>G	NP_001373232.1:p.Thr460Ala
NM_001386304.1:c.1276A>G	NP_001373233.1:p.Thr426Ala
NM_001386305.1:c.1240A>G	NP_001373234.1:p.Thr414Ala
NM_001386306.1:c.1081A>G	NP_001373235.1:p.Thr361Ala