Canonical Allele Identifier: CA380181683
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44286666C>T (hg19) chr11:g.44265116C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265116C>T , CM000673.2:g.44265116C>T GRCh38
NC_000011.9:g.44286666C>T , CM000673.1:g.44286666C>T GRCh37
NC_000011.8:g.44243242C>T NCBI36
NG_015809.1:g.50051G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.974G>A MANE Select ENSP00000498217.1:p.Cys325Tyr
ENST00000329255.3:c.974G>A ENSP00000332744.3:p.Cys325Tyr
NM_021926.3:c.974G>A NP_068745.2:p.Cys325Tyr
XM_011520265.1:c.452G>A XP_011518567.1:p.Cys151Tyr
XM_011520266.1:c.452G>A XP_011518568.1:p.Cys151Tyr
NM_021926.4:c.974G>A MANE Select NP_068745.2:p.Cys325Tyr
Search 100 bp 5'
Search 100 bp 3'