Canonical Allele Identifier: CA917262306

Gene: ADH4

Linked Data

• dbSNP Id: rs1560775007
• gnomAD v4: 4-99127309-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127313del , CM000666.2:g.99127313del	GRCh38
NC_000004.11:g.100048464del , CM000666.1:g.100048464del	GRCh37
NC_000004.10:g.100267487del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.878del MANE Select	ENSP00000265512.7:p.Gly293AspfsTer8
ENST00000265512.11:c.878del	ENSP00000265512.7:p.Gly293AspfsTer8
ENST00000505590.5:c.935del	ENSP00000425416.1:p.Gly312AspfsTer8
ENST00000506705.5:c.*852del	ENSP00000426667.1:n.*852del
ENST00000508393.5:c.935del	ENSP00000424630.1:p.Gly312AspfsTer8
ENST00000509471.5:c.334-578del	ENSP00000424583.1:n.334-578del
ENST00000629236.2:c.878del	ENSP00000486450.1:p.Gly293AspfsTer8
NM_000670.3:c.878del	NP_000661.2:p.Gly293AspfsTer8
NM_000670.4:c.878del	NP_000661.2:p.Gly293AspfsTer8
NM_001306171.1:c.935del	NP_001293100.1:p.Gly312AspfsTer8
NM_001306172.1:c.935del	NP_001293101.1:p.Gly312AspfsTer8
NR_037884.1:n.429-6242del
XR_938685.1:n.1106del
XR_938686.1:n.1097del
XR_938687.1:n.970del
NM_000670.5:c.878del MANE Select	NP_000661.2:p.Gly293AspfsTer8
NM_001306171.2:c.935del	NP_001293100.1:p.Gly312AspfsTer8
NM_001306172.2:c.935del	NP_001293101.1:p.Gly312AspfsTer8