Canonical Allele Identifier: CA2674977119

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119452484-T-TCCCGCCCCCGCCATTC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452491_119452506dup , CM000667.2:g.119452491_119452506dup	GRCh38
NC_000005.9:g.118788186_118788201dup , CM000667.1:g.118788186_118788201dup	GRCh37
NC_000005.8:g.118816085_118816100dup	NCBI36
NG_008182.1:g.5039_5054dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-85_-70dup	ENSP00000426272.2:n.-85_-70dup
ENST00000682996.1:c.-85_-70dup	ENSP00000507792.1:n.-85_-70dup
ENST00000683936.1:c.-85_-70dup	ENSP00000507721.1:n.-85_-70dup
ENST00000684214.1:c.-85_-70dup	ENSP00000508071.1:n.-85_-70dup
ENST00000256216.10:c.-85_-70dup	ENSP00000256216.6:n.-85_-70dup
ENST00000511186.5:n.19_34dup
NM_000414.3:c.-85_-70dup	NP_000405.1:n.-85_-70dup
NM_001199292.1:c.-85_-70dup	NP_001186221.1:n.-85_-70dup
NM_001292027.1:c.-222_-207dup	NP_001278956.1:n.-222_-207dup