Canonical Allele Identifier: CA474035380
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44286662G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44265112G>A , CM000673.2:g.44265112G>A GRCh38
NC_000011.9:g.44286662G>A , CM000673.1:g.44286662G>A GRCh37
NC_000011.8:g.44243238G>A NCBI36
NG_015809.1:g.50055C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.978C>T MANE Select ENSP00000498217.1:p.Asp326=
ENST00000329255.3:c.978C>T ENSP00000332744.3:p.Asp326=
NM_021926.3:c.978C>T NP_068745.2:p.Asp326=
XM_011520265.1:c.456C>T XP_011518567.1:p.Asp152=
XM_011520266.1:c.456C>T XP_011518568.1:p.Asp152=
NM_021926.4:c.978C>T MANE Select NP_068745.2:p.Asp326=
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