Canonical Allele Identifier: CA2671507044

Gene: ADH4

Linked Data

• gnomAD v4: 4-99127149-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127150_99127151del , CM000666.2:g.99127150_99127151del	GRCh38
NC_000004.11:g.100048301_100048302del , CM000666.1:g.100048301_100048302del	GRCh37
NC_000004.10:g.100267324_100267325del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.979+58_979+59del MANE Select	ENSP00000265512.7:n.979+58_979+59del
ENST00000265512.11:c.979+58_979+59del	ENSP00000265512.7:n.979+58_979+59del
ENST00000505590.5:c.1036+58_1036+59del	ENSP00000425416.1:n.1036+58_1036+59del
ENST00000506705.5:c.*953+58_*953+59del	ENSP00000426667.1:n.*953+58_*953+59del
ENST00000508393.5:c.1036+58_1036+59del	ENSP00000424630.1:n.1036+58_1036+59del
ENST00000509471.5:c.334-419_334-418del	ENSP00000424583.1:n.334-419_334-418del
ENST00000629236.2:c.979+58_979+59del	ENSP00000486450.1:n.979+58_979+59del
NM_000670.3:c.979+58_979+59del	NP_000661.2:n.979+58_979+59del
NM_000670.4:c.979+58_979+59del	NP_000661.2:n.979+58_979+59del
NM_001306171.1:c.1036+58_1036+59del	NP_001293100.1:n.1036+58_1036+59del
NM_001306172.1:c.1036+58_1036+59del	NP_001293101.1:n.1036+58_1036+59del
NR_037884.1:n.429-6405_429-6404del
XR_938685.1:n.1207+58_1207+59del
XR_938686.1:n.1198+58_1198+59del
XR_938687.1:n.1071+58_1071+59del
NM_000670.5:c.979+58_979+59del MANE Select	NP_000661.2:n.979+58_979+59del
NM_001306171.2:c.1036+58_1036+59del	NP_001293100.1:n.1036+58_1036+59del
NM_001306172.2:c.1036+58_1036+59del	NP_001293101.1:n.1036+58_1036+59del