Canonical Allele Identifier: CA380182202
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44296933C>A (hg19) chr11:g.44275383C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275383C>A , CM000673.2:g.44275383C>A GRCh38
NC_000011.9:g.44296933C>A , CM000673.1:g.44296933C>A GRCh37
NC_000011.8:g.44253509C>A NCBI36
NG_015809.1:g.39784G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.742G>T MANE Select ENSP00000498217.1:p.Ala248Ser
ENST00000329255.3:c.742G>T ENSP00000332744.3:p.Ala248Ser
NM_021926.3:c.742G>T NP_068745.2:p.Ala248Ser
XM_011520264.1:c.742G>T XP_011518566.1:p.Ala248Ser
XM_011520265.1:c.220G>T XP_011518567.1:p.Ala74Ser
XM_011520266.1:c.220G>T XP_011518568.1:p.Ala74Ser
NM_021926.4:c.742G>T MANE Select NP_068745.2:p.Ala248Ser
Search 100 bp 5'
Search 100 bp 3'