Canonical Allele Identifier: CA553095870

Gene: ADH4

Linked Data

• dbSNP Id: rs1338477427
• gnomAD v2: 4-100048239-T-TGA
• gnomAD v3: 4-99127088-T-TGA
• gnomAD v4: 4-99127088-T-TGA
• MyVariant Identifiers: chr4:g.100048239_100048240insGA (hg19) ; chr4:g.99127088_99127089insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127088_99127089insGA , CM000666.2:g.99127088_99127089insGA	GRCh38
NC_000004.11:g.100048239_100048240insGA , CM000666.1:g.100048239_100048240insGA	GRCh37
NC_000004.10:g.100267262_100267263insGA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.979+120_979+121insTC MANE Select	ENSP00000265512.7:n.979+120_979+121insTC
ENST00000265512.11:c.979+120_979+121insTC	ENSP00000265512.7:n.979+120_979+121insTC
ENST00000505590.5:c.1036+120_1036+121insTC	ENSP00000425416.1:n.1036+120_1036+121insTC
ENST00000506705.5:c.*953+120_*953+121insTC	ENSP00000426667.1:n.*953+120_*953+121insTC
ENST00000508393.5:c.1036+120_1036+121insTC	ENSP00000424630.1:n.1036+120_1036+121insTC
ENST00000509471.5:c.334-357_334-356insTC	ENSP00000424583.1:n.334-357_334-356insTC
ENST00000629236.2:c.979+120_979+121insTC	ENSP00000486450.1:n.979+120_979+121insTC
NM_000670.3:c.979+120_979+121insTC	NP_000661.2:n.979+120_979+121insTC
NM_000670.4:c.979+120_979+121insTC	NP_000661.2:n.979+120_979+121insTC
NM_001306171.1:c.1036+120_1036+121insTC	NP_001293100.1:n.1036+120_1036+121insTC
NM_001306172.1:c.1036+120_1036+121insTC	NP_001293101.1:n.1036+120_1036+121insTC
NR_037884.1:n.429-6467_429-6466insGA
XR_938685.1:n.1207+120_1207+121insTC
XR_938686.1:n.1198+120_1198+121insTC
XR_938687.1:n.1071+120_1071+121insTC
NM_000670.5:c.979+120_979+121insTC MANE Select	NP_000661.2:n.979+120_979+121insTC
NM_001306171.2:c.1036+120_1036+121insTC	NP_001293100.1:n.1036+120_1036+121insTC
NM_001306172.2:c.1036+120_1036+121insTC	NP_001293101.1:n.1036+120_1036+121insTC