Canonical Allele Identifier: CA2674977134

Gene: HSD17B4

Linked Data

• gnomAD v4: 5-119452499-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.119452503del , CM000667.2:g.119452503del	GRCh38
NC_000005.9:g.118788198del , CM000667.1:g.118788198del	GRCh37
NC_000005.8:g.118816097del	NCBI36
NG_008182.1:g.5051del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000509514.6:c.-73del	ENSP00000426272.2:n.-73del
ENST00000682996.1:c.-73del	ENSP00000507792.1:n.-73del
ENST00000683936.1:c.-73del	ENSP00000507721.1:n.-73del
ENST00000683974.1:n.10del
ENST00000684214.1:c.-73del	ENSP00000508071.1:n.-73del
ENST00000414835.7:c.-251del	ENSP00000411960.3:n.-251del
ENST00000510025.7:c.-73del MANE Select	ENSP00000424940.3:n.-73del
ENST00000646590.1:c.-73del	ENSP00000494892.1:n.-73del
ENST00000256216.10:c.-73del	ENSP00000256216.6:n.-73del
ENST00000442060.7:c.-73del	ENSP00000390208.3:n.-73del
ENST00000511186.5:n.31del
ENST00000515320.5:c.-73del	ENSP00000424613.1:n.-73del
NM_000414.3:c.-73del	NP_000405.1:n.-73del
NM_001199291.2:c.-251del	NP_001186220.1:n.-251del
NM_001199292.1:c.-73del	NP_001186221.1:n.-73del
NM_001292027.1:c.-210del	NP_001278956.1:n.-210del
NM_001292028.1:c.-672del	NP_001278957.1:n.-672del
NM_000414.4:c.-73del MANE Select	NP_000405.1:n.-73del
NM_001199291.3:c.-251del	NP_001186220.1:n.-251del
NM_001199292.2:c.-73del	NP_001186221.1:n.-73del
NM_001292027.2:c.-210del	NP_001278956.1:n.-210del
NM_001292028.2:c.-672del	NP_001278957.1:n.-672del
NM_001374497.1:c.-73del	NP_001361426.1:n.-73del
NM_001374498.1:c.-73del	NP_001361427.1:n.-73del
NM_001374499.1:c.-606del	NP_001361428.1:n.-606del
NM_001374500.1:c.-799del	NP_001361429.1:n.-799del
NM_001374501.1:c.-672del	NP_001361430.1:n.-672del
NM_001374502.1:c.-677del	NP_001361431.1:n.-677del
NM_001374503.1:c.-742del	NP_001361432.1:n.-742del
NR_164653.1:n.7del
NR_164654.1:n.7del