Canonical Allele Identifier: CA473833866
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296931G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275381G>C , CM000673.2:g.44275381G>C GRCh38
NC_000011.9:g.44296931G>C , CM000673.1:g.44296931G>C GRCh37
NC_000011.8:g.44253507G>C NCBI36
NG_015809.1:g.39786C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.744C>G MANE Select ENSP00000498217.1:p.Ala248=
ENST00000329255.3:c.744C>G ENSP00000332744.3:p.Ala248=
NM_021926.3:c.744C>G NP_068745.2:p.Ala248=
XM_011520264.1:c.744C>G XP_011518566.1:p.Ala248=
XM_011520265.1:c.222C>G XP_011518567.1:p.Ala74=
XM_011520266.1:c.222C>G XP_011518568.1:p.Ala74=
NM_021926.4:c.744C>G MANE Select NP_068745.2:p.Ala248=