Canonical Allele Identifier: CA380182233
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296948C>T (hg19) chr11:g.44275398C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275398C>T , CM000673.2:g.44275398C>T GRCh38
NC_000011.9:g.44296948C>T , CM000673.1:g.44296948C>T GRCh37
NC_000011.8:g.44253524C>T NCBI36
NG_015809.1:g.39769G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.727G>A MANE Select ENSP00000498217.1:p.Ala243Thr
ENST00000329255.3:c.727G>A ENSP00000332744.3:p.Ala243Thr
NM_021926.3:c.727G>A NP_068745.2:p.Ala243Thr
XM_011520264.1:c.727G>A XP_011518566.1:p.Ala243Thr
XM_011520265.1:c.205G>A XP_011518567.1:p.Ala69Thr
XM_011520266.1:c.205G>A XP_011518568.1:p.Ala69Thr
NM_021926.4:c.727G>A MANE Select NP_068745.2:p.Ala243Thr
Search 100 bp 5'
Search 100 bp 3'