Canonical Allele Identifier: CA1479859499

Gene: ADH4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99124567_99124568delinsCT , CM000666.2:g.99124567_99124568delinsCT	GRCh38
NC_000004.11:g.100045718_100045719delinsCT , CM000666.1:g.100045718_100045719delinsCT	GRCh37
NC_000004.10:g.100264741_100264742delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.1119-102_1119-101delinsAG MANE Select	ENSP00000265512.7:n.1119-102_1119-101delinsAG
ENST00000265512.11:c.1119-102_1119-101delinsAG	ENSP00000265512.7:n.1119-102_1119-101delinsAG
ENST00000505590.5:c.1176-102_1176-101delinsAG	ENSP00000425416.1:n.1176-102_1176-101delinsAG
ENST00000508393.5:c.1176-102_1176-101delinsAG	ENSP00000424630.1:n.1176-102_1176-101delinsAG
ENST00000509471.5:c.473-102_473-101delinsAG	ENSP00000424583.1:n.473-102_473-101delinsAG
ENST00000629236.2:c.1119-102_1119-101delinsAG	ENSP00000486450.1:n.1119-102_1119-101delinsAG
NM_000670.3:c.1119-102_1119-101delinsAG	NP_000661.2:n.1119-102_1119-101delinsAG
NM_000670.4:c.1119-102_1119-101delinsAG	NP_000661.2:n.1119-102_1119-101delinsAG
NM_001306171.1:c.1176-102_1176-101delinsAG	NP_001293100.1:n.1176-102_1176-101delinsAG
NM_001306172.1:c.1176-102_1176-101delinsAG	NP_001293101.1:n.1176-102_1176-101delinsAG
NR_037884.1:n.429-8988_429-8987delinsCT
XR_938685.1:n.1458-102_1458-101delinsAG
XR_938686.1:n.1449-102_1449-101delinsAG
XR_938687.1:n.1322-102_1322-101delinsAG
NM_000670.5:c.1119-102_1119-101delinsAG MANE Select	NP_000661.2:n.1119-102_1119-101delinsAG
NM_001306171.2:c.1176-102_1176-101delinsAG	NP_001293100.1:n.1176-102_1176-101delinsAG
NM_001306172.2:c.1176-102_1176-101delinsAG	NP_001293101.1:n.1176-102_1176-101delinsAG