Canonical Allele Identifier: CA357479945

Gene: ADH4

Linked Data

• MyVariant Identifiers: chr4:g.100048461C>A (hg19) ; chr4:g.99127310C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.99127310C>A , CM000666.2:g.99127310C>A	GRCh38
NC_000004.11:g.100048461C>A , CM000666.1:g.100048461C>A	GRCh37
NC_000004.10:g.100267484C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265512.12:c.878G>T MANE Select	ENSP00000265512.7:p.Gly293Val
ENST00000265512.11:c.878G>T	ENSP00000265512.7:p.Gly293Val
ENST00000505590.5:c.935G>T	ENSP00000425416.1:p.Gly312Val
ENST00000506705.5:c.*852G>T	ENSP00000426667.1:n.*852G>T
ENST00000508393.5:c.935G>T	ENSP00000424630.1:p.Gly312Val
ENST00000509471.5:c.334-578G>T	ENSP00000424583.1:n.334-578G>T
ENST00000629236.2:c.878G>T	ENSP00000486450.1:p.Gly293Val
NM_000670.3:c.878G>T	NP_000661.2:p.Gly293Val
NM_000670.4:c.878G>T	NP_000661.2:p.Gly293Val
NM_001306171.1:c.935G>T	NP_001293100.1:p.Gly312Val
NM_001306172.1:c.935G>T	NP_001293101.1:p.Gly312Val
NR_037884.1:n.429-6245C>A
XR_938685.1:n.1106G>T
XR_938686.1:n.1097G>T
XR_938687.1:n.970G>T
NM_000670.5:c.878G>T MANE Select	NP_000661.2:p.Gly293Val
NM_001306171.2:c.935G>T	NP_001293100.1:p.Gly312Val
NM_001306172.2:c.935G>T	NP_001293101.1:p.Gly312Val