Canonical Allele Identifier: CA1479859543
Gene: ADH4 HGNC NCBI

Linked Data

dbSNP Id: rs1729026165

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99124680_99124681del , CM000666.2:g.99124680_99124681del GRCh38
NC_000004.11:g.100045831_100045832del , CM000666.1:g.100045831_100045832del GRCh37
NC_000004.10:g.100264854_100264855del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.1119-215_1119-214del MANE Select ENSP00000265512.7:n.1119-215_1119-214del
ENST00000265512.11:c.1119-215_1119-214del ENSP00000265512.7:n.1119-215_1119-214del
ENST00000505590.5:c.1176-215_1176-214del ENSP00000425416.1:n.1176-215_1176-214del
ENST00000508393.5:c.1176-215_1176-214del ENSP00000424630.1:n.1176-215_1176-214del
ENST00000509471.5:c.473-215_473-214del ENSP00000424583.1:n.473-215_473-214del
ENST00000629236.2:c.1119-215_1119-214del ENSP00000486450.1:n.1119-215_1119-214del
NM_000670.3:c.1119-215_1119-214del NP_000661.2:n.1119-215_1119-214del
NM_000670.4:c.1119-215_1119-214del NP_000661.2:n.1119-215_1119-214del
NM_001306171.1:c.1176-215_1176-214del NP_001293100.1:n.1176-215_1176-214del
NM_001306172.1:c.1176-215_1176-214del NP_001293101.1:n.1176-215_1176-214del
NR_037884.1:n.429-8875_429-8874del
XR_938685.1:n.1457+11_1457+12del
XR_938686.1:n.1448+11_1448+12del
XR_938687.1:n.1321+11_1321+12del
NM_000670.5:c.1119-215_1119-214del MANE Select NP_000661.2:n.1119-215_1119-214del
NM_001306171.2:c.1176-215_1176-214del NP_001293100.1:n.1176-215_1176-214del
NM_001306172.2:c.1176-215_1176-214del NP_001293101.1:n.1176-215_1176-214del