Canonical Allele Identifier: CA101609283

Gene: ADH4

Linked Data

• dbSNP Id: rs552034371
• MyVariant Identifiers: chr4:g.100055518_100055520del (hg19) ; chr4:g.99134367_99134369del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99134370_99134372del , CM000666.2:g.99134370_99134372del	GRCh38
NC_000004.11:g.100055521_100055523del , CM000666.1:g.100055521_100055523del	GRCh37
NC_000004.10:g.100274544_100274546del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000265512.12:c.582+2097_582+2099del MANE Select	ENSP00000265512.7:n.582+2097_582+2099del
ENST00000265512.11:c.582+2097_582+2099del	ENSP00000265512.7:n.582+2097_582+2099del
ENST00000503416.5:n.595+2097_595+2099del
ENST00000504125.1:c.528+2097_528+2099del	ENSP00000427525.1:n.528+2097_528+2099del
ENST00000505590.5:c.639+2097_639+2099del	ENSP00000425416.1:n.639+2097_639+2099del
ENST00000506705.5:c.*556+2097_*556+2099del	ENSP00000426667.1:n.*556+2097_*556+2099de...
ENST00000508393.5:c.639+2097_639+2099del	ENSP00000424630.1:n.639+2097_639+2099del
ENST00000509471.5:c.72+2097_72+2099del	ENSP00000424583.1:n.72+2097_72+2099del
ENST00000512499.5:c.639+2097_639+2099del	ENSP00000423571.1:n.639+2097_639+2099del
ENST00000629236.2:c.582+2097_582+2099del	ENSP00000486450.1:n.582+2097_582+2099del
NM_000670.3:c.582+2097_582+2099del	NP_000661.2:n.582+2097_582+2099del
NM_000670.4:c.582+2097_582+2099del	NP_000661.2:n.582+2097_582+2099del
NM_001306171.1:c.639+2097_639+2099del	NP_001293100.1:n.639+2097_639+2099del
NM_001306172.1:c.639+2097_639+2099del	NP_001293101.1:n.639+2097_639+2099del
NR_037884.1:n.679+565_679+567del
XR_938685.1:n.810+2097_810+2099del
XR_938686.1:n.801+2097_801+2099del
XR_938687.1:n.674+2097_674+2099del
NM_000670.5:c.582+2097_582+2099del MANE Select	NP_000661.2:n.582+2097_582+2099del
NM_001306171.2:c.639+2097_639+2099del	NP_001293100.1:n.639+2097_639+2099del
NM_001306172.2:c.639+2097_639+2099del	NP_001293101.1:n.639+2097_639+2099del