Canonical Allele Identifier: CA471745335

Gene: HTRA1

Linked Data

• gnomAD v4: 10-122461685-G-T
• MyVariant Identifiers: chr10:g.124221201G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122461685G>T , CM000672.2:g.122461685G>T	GRCh38
NC_000010.10:g.124221201G>T , CM000672.1:g.124221201G>T	GRCh37
NC_000010.9:g.124211191G>T	NCBI36
NG_011554.1:g.5161G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.33G>T MANE Select	ENSP00000357980.3:p.Leu11=
ENST00000648167.1:c.154+2976G>T	ENSP00000498033.1:n.154+2976G>T
ENST00000368984.7:c.33G>T	ENSP00000357980.3:p.Leu11=
NM_002775.4:c.33G>T	NP_002766.1:p.Leu11=
NM_002775.5:c.33G>T MANE Select	NP_002766.1:p.Leu11=