Canonical Allele Identifier: CA378585428

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124266260G>T (hg19) ; chr10:g.122506744G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506744G>T , CM000672.2:g.122506744G>T	GRCh38
NC_000010.10:g.124266260G>T , CM000672.1:g.124266260G>T	GRCh37
NC_000010.9:g.124256250G>T	NCBI36
NG_011554.1:g.50220G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.831G>T MANE Select	ENSP00000357980.3:p.Glu277Asp
ENST00000648167.1:c.513G>T	ENSP00000498033.1:p.Glu171Asp
ENST00000368984.7:c.831G>T	ENSP00000357980.3:p.Glu277Asp
ENST00000420892.1:c.54G>T	ENSP00000412676.1:p.Glu18Asp
NM_002775.4:c.831G>T	NP_002766.1:p.Glu277Asp
NM_002775.5:c.831G>T MANE Select	NP_002766.1:p.Glu277Asp