Canonical Allele Identifier: CA101602182

Gene: ADH4

Linked Data

• dbSNP Id: rs1553954893
• MyVariant Identifiers: chr4:g.100047448_100047449insATT (hg19) ; chr4:g.99126297_99126298insATT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99126297_99126298insATT , CM000666.2:g.99126297_99126298insATT	GRCh38
NC_000004.11:g.100047448_100047449insATT , CM000666.1:g.100047448_100047449insATT	GRCh37
NC_000004.10:g.100266471_100266472insATT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1118+296_1118+297insAAT MANE Select	ENSP00000265512.7:n.1118+296_1118+297insAAT
ENST00000265512.11:c.1118+296_1118+297insAAT	ENSP00000265512.7:n.1118+296_1118+297insAAT
ENST00000505590.5:c.1175+296_1175+297insAAT	ENSP00000425416.1:n.1175+296_1175+297insAAT
ENST00000508393.5:c.1175+296_1175+297insAAT	ENSP00000424630.1:n.1175+296_1175+297insAAT
ENST00000509471.5:c.472+296_472+297insAAT	ENSP00000424583.1:n.472+296_472+297insAAT
ENST00000629236.2:c.1118+296_1118+297insAAT	ENSP00000486450.1:n.1118+296_1118+297insAAT
NM_000670.3:c.1118+296_1118+297insAAT	NP_000661.2:n.1118+296_1118+297insAAT
NM_000670.4:c.1118+296_1118+297insAAT	NP_000661.2:n.1118+296_1118+297insAAT
NM_001306171.1:c.1175+296_1175+297insAAT	NP_001293100.1:n.1175+296_1175+297insAAT
NM_001306172.1:c.1175+296_1175+297insAAT	NP_001293101.1:n.1175+296_1175+297insAAT
NR_037884.1:n.429-7258_429-7257insATT
XR_938685.1:n.1346+296_1346+297insAAT
XR_938686.1:n.1337+296_1337+297insAAT
XR_938687.1:n.1210+296_1210+297insAAT
NM_000670.5:c.1118+296_1118+297insAAT MANE Select	NP_000661.2:n.1118+296_1118+297insAAT
NM_001306171.2:c.1175+296_1175+297insAAT	NP_001293100.1:n.1175+296_1175+297insAAT
NM_001306172.2:c.1175+296_1175+297insAAT	NP_001293101.1:n.1175+296_1175+297insAAT