Canonical Allele Identifier: CA1941478150

Gene: HTRA1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122508805_122508806delinsAG , CM000672.2:g.122508805_122508806delinsAG	GRCh38
NC_000010.10:g.124268321_124268322delinsAG , CM000672.1:g.124268321_124268322delinsAG	GRCh37
NC_000010.9:g.124258311_124258312delinsAG	NCBI36
NG_011554.1:g.52281_52282delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.1120+35_1120+36delinsAG MANE Select	ENSP00000357980.3:n.1120+35_1120+36delinsAG
ENST00000648167.1:c.802+35_802+36delinsAG	ENSP00000498033.1:n.802+35_802+36delinsAG
ENST00000368984.7:c.1120+35_1120+36delinsAG	ENSP00000357980.3:n.1120+35_1120+36delinsAG
ENST00000420892.1:c.343+35_343+36delinsAG	ENSP00000412676.1:n.343+35_343+36delinsAG
NM_002775.4:c.1120+35_1120+36delinsAG	NP_002766.1:n.1120+35_1120+36delinsAG
NM_002775.5:c.1120+35_1120+36delinsAG MANE Select	NP_002766.1:n.1120+35_1120+36delinsAG