Canonical Allele Identifier: CA800706612

Gene: ADH4

Linked Data

• dbSNP Id: rs1264356744
• gnomAD v4: 4-99127203-A-AG
• MyVariant Identifiers: chr4:g.100048354_100048355insG (hg19) ; chr4:g.99127203_99127204insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127203_99127204insG , CM000666.2:g.99127203_99127204insG	GRCh38
NC_000004.11:g.100048354_100048355insG , CM000666.1:g.100048354_100048355insG	GRCh37
NC_000004.10:g.100267377_100267378insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+5_979+6insC MANE Select	ENSP00000265512.7:n.979+5_979+6insC
ENST00000265512.11:c.979+5_979+6insC	ENSP00000265512.7:n.979+5_979+6insC
ENST00000505590.5:c.1036+5_1036+6insC	ENSP00000425416.1:n.1036+5_1036+6insC
ENST00000506705.5:c.*953+5_*953+6insC	ENSP00000426667.1:n.*953+5_*953+6insC
ENST00000508393.5:c.1036+5_1036+6insC	ENSP00000424630.1:n.1036+5_1036+6insC
ENST00000509471.5:c.334-472_334-471insC	ENSP00000424583.1:n.334-472_334-471insC
ENST00000629236.2:c.979+5_979+6insC	ENSP00000486450.1:n.979+5_979+6insC
NM_000670.3:c.979+5_979+6insC	NP_000661.2:n.979+5_979+6insC
NM_000670.4:c.979+5_979+6insC	NP_000661.2:n.979+5_979+6insC
NM_001306171.1:c.1036+5_1036+6insC	NP_001293100.1:n.1036+5_1036+6insC
NM_001306172.1:c.1036+5_1036+6insC	NP_001293101.1:n.1036+5_1036+6insC
NR_037884.1:n.429-6352_429-6351insG
XR_938685.1:n.1207+5_1207+6insC
XR_938686.1:n.1198+5_1198+6insC
XR_938687.1:n.1071+5_1071+6insC
NM_000670.5:c.979+5_979+6insC MANE Select	NP_000661.2:n.979+5_979+6insC
NM_001306171.2:c.1036+5_1036+6insC	NP_001293100.1:n.1036+5_1036+6insC
NM_001306172.2:c.1036+5_1036+6insC	NP_001293101.1:n.1036+5_1036+6insC