Canonical Allele Identifier: CA1479860281

Gene: ADH4

Linked Data

• dbSNP Id: rs1729088116

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126318_99126321del , CM000666.2:g.99126318_99126321del	GRCh38
NC_000004.11:g.100047469_100047472del , CM000666.1:g.100047469_100047472del	GRCh37
NC_000004.10:g.100266492_100266495del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+276_1118+279del MANE Select	ENSP00000265512.7:n.1118+276_1118+279del
ENST00000265512.11:c.1118+276_1118+279del	ENSP00000265512.7:n.1118+276_1118+279del
ENST00000505590.5:c.1175+276_1175+279del	ENSP00000425416.1:n.1175+276_1175+279del
ENST00000508393.5:c.1175+276_1175+279del	ENSP00000424630.1:n.1175+276_1175+279del
ENST00000509471.5:c.472+276_472+279del	ENSP00000424583.1:n.472+276_472+279del
ENST00000629236.2:c.1118+276_1118+279del	ENSP00000486450.1:n.1118+276_1118+279del
NM_000670.3:c.1118+276_1118+279del	NP_000661.2:n.1118+276_1118+279del
NM_000670.4:c.1118+276_1118+279del	NP_000661.2:n.1118+276_1118+279del
NM_001306171.1:c.1175+276_1175+279del	NP_001293100.1:n.1175+276_1175+279del
NM_001306172.1:c.1175+276_1175+279del	NP_001293101.1:n.1175+276_1175+279del
NR_037884.1:n.429-7237_429-7234del
XR_938685.1:n.1346+276_1346+279del
XR_938686.1:n.1337+276_1337+279del
XR_938687.1:n.1210+276_1210+279del
NM_000670.5:c.1118+276_1118+279del MANE Select	NP_000661.2:n.1118+276_1118+279del
NM_001306171.2:c.1175+276_1175+279del	NP_001293100.1:n.1175+276_1175+279del
NM_001306172.2:c.1175+276_1175+279del	NP_001293101.1:n.1175+276_1175+279del