Canonical Allele Identifier: CA1941477358

Gene: HTRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122507082G= , CM000672.2:g.122507082G=	GRCh38
NC_000010.10:g.124266598G= , CM000672.1:g.124266598G=	GRCh37
NC_000010.9:g.124256588G=	NCBI36
NG_011554.1:g.50558G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.972+197G= MANE Select	ENSP00000357980.3:n.972+197G=
ENST00000648167.1:c.654+197G=	ENSP00000498033.1:n.654+197G=
ENST00000368984.7:c.972+197G=	ENSP00000357980.3:n.972+197G=
ENST00000420892.1:c.195+197G=	ENSP00000412676.1:n.195+197G=
NM_002775.4:c.972+197G=	NP_002766.1:n.972+197G=
NM_002775.5:c.972+197G= MANE Select	NP_002766.1:n.972+197G=