Canonical Allele Identifier: CA378586949

Gene: HTRA1

Linked Data

• dbSNP Id: rs1446690333
• MyVariant Identifiers: chr10:g.124268280G>T (hg19) ; chr10:g.122508764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122508764G>T , CM000672.2:g.122508764G>T	GRCh38
NC_000010.10:g.124268280G>T , CM000672.1:g.124268280G>T	GRCh37
NC_000010.9:g.124258270G>T	NCBI36
NG_011554.1:g.52240G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368984.8:c.1114G>T MANE Select	ENSP00000357980.3:p.Ala372Ser
ENST00000648167.1:c.796G>T	ENSP00000498033.1:p.Ala266Ser
ENST00000368984.7:c.1114G>T	ENSP00000357980.3:p.Ala372Ser
ENST00000420892.1:c.337G>T	ENSP00000412676.1:p.Ala113Ser
NM_002775.4:c.1114G>T	NP_002766.1:p.Ala372Ser
NM_002775.5:c.1114G>T MANE Select	NP_002766.1:p.Ala372Ser