Canonical Allele Identifier: CA101602722

Gene: ADH4

Linked Data

• dbSNP Id: rs949013390
• gnomAD v2: 4-100048037-ATT-A
• gnomAD v3: 4-99126886-ATT-A
• gnomAD v4: 4-99126886-ATT-A
• MyVariant Identifiers: chr4:g.100048038_100048039del (hg19) ; chr4:g.99126887_99126888del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126889_99126890del , CM000666.2:g.99126889_99126890del	GRCh38
NC_000004.11:g.100048040_100048041del , CM000666.1:g.100048040_100048041del	GRCh37
NC_000004.10:g.100267063_100267064del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.980-156_980-155del MANE Select	ENSP00000265512.7:n.980-156_980-155del
ENST00000265512.11:c.980-156_980-155del	ENSP00000265512.7:n.980-156_980-155del
ENST00000505590.5:c.1037-156_1037-155del	ENSP00000425416.1:n.1037-156_1037-155del
ENST00000506705.5:c.*954-156_*954-155del	ENSP00000426667.1:n.*954-156_*954-155del
ENST00000508393.5:c.1037-156_1037-155del	ENSP00000424630.1:n.1037-156_1037-155del
ENST00000509471.5:c.334-156_334-155del	ENSP00000424583.1:n.334-156_334-155del
ENST00000629236.2:c.980-156_980-155del	ENSP00000486450.1:n.980-156_980-155del
NM_000670.3:c.980-156_980-155del	NP_000661.2:n.980-156_980-155del
NM_000670.4:c.980-156_980-155del	NP_000661.2:n.980-156_980-155del
NM_001306171.1:c.1037-156_1037-155del	NP_001293100.1:n.1037-156_1037-155del
NM_001306172.1:c.1037-156_1037-155del	NP_001293101.1:n.1037-156_1037-155del
NR_037884.1:n.429-6666_429-6665del
XR_938685.1:n.1208-156_1208-155del
XR_938686.1:n.1199-156_1199-155del
XR_938687.1:n.1072-156_1072-155del
NM_000670.5:c.980-156_980-155del MANE Select	NP_000661.2:n.980-156_980-155del
NM_001306171.2:c.1037-156_1037-155del	NP_001293100.1:n.1037-156_1037-155del
NM_001306172.2:c.1037-156_1037-155del	NP_001293101.1:n.1037-156_1037-155del