Canonical Allele Identifier: CA101603057

Gene: ADH4

Linked Data

• dbSNP Id: rs928612218
• gnomAD v2: 4-100048440-ACTC-A
• gnomAD v3: 4-99127289-ACTC-A
• gnomAD v4: 4-99127289-ACTC-A
• MyVariant Identifiers: chr4:g.100048441_100048443del (hg19) ; chr4:g.99127290_99127292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127291_99127293del , CM000666.2:g.99127291_99127293del	GRCh38
NC_000004.11:g.100048442_100048444del , CM000666.1:g.100048442_100048444del	GRCh37
NC_000004.10:g.100267465_100267467del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.896_898del MANE Select	ENSP00000265512.7:p.Gly299del
ENST00000265512.11:c.896_898del	ENSP00000265512.7:p.Gly299del
ENST00000505590.5:c.953_955del	ENSP00000425416.1:p.Gly318del
ENST00000506705.5:c.*870_*872del	ENSP00000426667.1:n.*870_*872del
ENST00000508393.5:c.953_955del	ENSP00000424630.1:p.Gly318del
ENST00000509471.5:c.334-560_334-558del	ENSP00000424583.1:n.334-560_334-558del
ENST00000629236.2:c.896_898del	ENSP00000486450.1:p.Gly299del
NM_000670.3:c.896_898del	NP_000661.2:p.Gly299del
NM_000670.4:c.896_898del	NP_000661.2:p.Gly299del
NM_001306171.1:c.953_955del	NP_001293100.1:p.Gly318del
NM_001306172.1:c.953_955del	NP_001293101.1:p.Gly318del
NR_037884.1:n.429-6264_429-6262del
XR_938685.1:n.1124_1126del
XR_938686.1:n.1115_1117del
XR_938687.1:n.988_990del
NM_000670.5:c.896_898del MANE Select	NP_000661.2:p.Gly299del
NM_001306171.2:c.953_955del	NP_001293100.1:p.Gly318del
NM_001306172.2:c.953_955del	NP_001293101.1:p.Gly318del