Canonical Allele Identifier: CA473833856
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296922T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275372T>G , CM000673.2:g.44275372T>G GRCh38
NC_000011.9:g.44296922T>G , CM000673.1:g.44296922T>G GRCh37
NC_000011.8:g.44253498T>G NCBI36
NG_015809.1:g.39795A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.753A>C MANE Select ENSP00000498217.1:p.Thr251=
ENST00000329255.3:c.753A>C ENSP00000332744.3:p.Thr251=
NM_021926.3:c.753A>C NP_068745.2:p.Thr251=
XM_011520264.1:c.753A>C XP_011518566.1:p.Thr251=
XM_011520265.1:c.231A>C XP_011518567.1:p.Thr77=
XM_011520266.1:c.231A>C XP_011518568.1:p.Thr77=
NM_021926.4:c.753A>C MANE Select NP_068745.2:p.Thr251=
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