Canonical Allele Identifier: CA101602192

Gene: ADH4

Linked Data

• dbSNP Id: rs869263014
• MyVariant Identifiers: chr4:g.100047450_100047451insTAT (hg19) ; chr4:g.99126299_99126300insTAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126299_99126300insTAT , CM000666.2:g.99126299_99126300insTAT	GRCh38
NC_000004.11:g.100047450_100047451insTAT , CM000666.1:g.100047450_100047451insTAT	GRCh37
NC_000004.10:g.100266473_100266474insTAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+294_1118+295insATA MANE Select	ENSP00000265512.7:n.1118+294_1118+295insATA
ENST00000265512.11:c.1118+294_1118+295insATA	ENSP00000265512.7:n.1118+294_1118+295insATA
ENST00000505590.5:c.1175+294_1175+295insATA	ENSP00000425416.1:n.1175+294_1175+295insATA
ENST00000508393.5:c.1175+294_1175+295insATA	ENSP00000424630.1:n.1175+294_1175+295insATA
ENST00000509471.5:c.472+294_472+295insATA	ENSP00000424583.1:n.472+294_472+295insATA
ENST00000629236.2:c.1118+294_1118+295insATA	ENSP00000486450.1:n.1118+294_1118+295insATA
NM_000670.3:c.1118+294_1118+295insATA	NP_000661.2:n.1118+294_1118+295insATA
NM_000670.4:c.1118+294_1118+295insATA	NP_000661.2:n.1118+294_1118+295insATA
NM_001306171.1:c.1175+294_1175+295insATA	NP_001293100.1:n.1175+294_1175+295insATA
NM_001306172.1:c.1175+294_1175+295insATA	NP_001293101.1:n.1175+294_1175+295insATA
NR_037884.1:n.429-7256_429-7255insTAT
XR_938685.1:n.1346+294_1346+295insATA
XR_938686.1:n.1337+294_1337+295insATA
XR_938687.1:n.1210+294_1210+295insATA
NM_000670.5:c.1118+294_1118+295insATA MANE Select	NP_000661.2:n.1118+294_1118+295insATA
NM_001306171.2:c.1175+294_1175+295insATA	NP_001293100.1:n.1175+294_1175+295insATA
NM_001306172.2:c.1175+294_1175+295insATA	NP_001293101.1:n.1175+294_1175+295insATA