Canonical Allele Identifier: CA2671507123
Gene: ADH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.99127356_99127357del , CM000666.2:g.99127356_99127357del GRCh38
NC_000004.11:g.100048507_100048508del , CM000666.1:g.100048507_100048508del GRCh37
NC_000004.10:g.100267530_100267531del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265512.12:c.844-13_844-12del MANE Select ENSP00000265512.7:n.844-13_844-12del
ENST00000265512.11:c.844-13_844-12del ENSP00000265512.7:n.844-13_844-12del
ENST00000505590.5:c.901-13_901-12del ENSP00000425416.1:n.901-13_901-12del
ENST00000506705.5:c.*818-13_*818-12del ENSP00000426667.1:n.*818-13_*818-12del
ENST00000508393.5:c.901-13_901-12del ENSP00000424630.1:n.901-13_901-12del
ENST00000509471.5:c.334-625_334-624del ENSP00000424583.1:n.334-625_334-624del
ENST00000629236.2:c.844-13_844-12del ENSP00000486450.1:n.844-13_844-12del
NM_000670.3:c.844-13_844-12del NP_000661.2:n.844-13_844-12del
NM_000670.4:c.844-13_844-12del NP_000661.2:n.844-13_844-12del
NM_001306171.1:c.901-13_901-12del NP_001293100.1:n.901-13_901-12del
NM_001306172.1:c.901-13_901-12del NP_001293101.1:n.901-13_901-12del
NR_037884.1:n.429-6199_429-6198del
XR_938685.1:n.1072-13_1072-12del
XR_938686.1:n.1063-13_1063-12del
XR_938687.1:n.936-13_936-12del
NM_000670.5:c.844-13_844-12del MANE Select NP_000661.2:n.844-13_844-12del
NM_001306171.2:c.901-13_901-12del NP_001293100.1:n.901-13_901-12del
NM_001306172.2:c.901-13_901-12del NP_001293101.1:n.901-13_901-12del