Canonical Allele Identifier: CA343773634

Gene: SERPINC1

Linked Data

• MyVariant Identifiers: chr1:g.173878768C>G (hg19) ; chr1:g.173909630C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909630C>G , CM000663.2:g.173909630C>G	GRCh38
NC_000001.10:g.173878768C>G , CM000663.1:g.173878768C>G	GRCh37
NC_000001.9:g.172145391C>G	NCBI36
NG_012462.1:g.12749G>C , LRG_577:g.12749G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1075G>C MANE Select	ENSP00000356671.3:p.Asp359His
ENST00000367698.3:c.1075G>C	ENSP00000356671.3:p.Asp359His
ENST00000617423.4:c.560-2137G>C	ENSP00000478688.1:n.560-2137G>C
NM_000488.3:c.1075G>C , LRG_577t1:c.1075G>C	NP_000479.1:p.Asp359His
XM_005245198.2:c.931G>C	XP_005245255.1:p.Asp311His
NM_001365052.1:c.931G>C	NP_001351981.1:p.Asp311His
NM_000488.4:c.1075G>C MANE Select	NP_000479.1:p.Asp359His
NM_001365052.2:c.931G>C	NP_001351981.1:p.Asp311His
NM_001386302.1:c.1198G>C	NP_001373231.1:p.Asp400His
NM_001386303.1:c.1156G>C	NP_001373232.1:p.Asp386His
NM_001386304.1:c.1054G>C	NP_001373233.1:p.Asp352His
NM_001386305.1:c.1018G>C	NP_001373234.1:p.Asp340His
NM_001386306.1:c.859G>C	NP_001373235.1:p.Asp287His