Canonical Allele Identifier: CA380182727
Gene: ALX4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44297178A>C (hg19) chr11:g.44275628A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275628A>C , CM000673.2:g.44275628A>C GRCh38
NC_000011.9:g.44297178A>C , CM000673.1:g.44297178A>C GRCh37
NC_000011.8:g.44253754A>C NCBI36
NG_015809.1:g.39539T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000652299.1:c.497T>G MANE Select ENSP00000498217.1:p.Leu166Ter
ENST00000329255.3:c.497T>G ENSP00000332744.3:p.Leu166Ter
NM_021926.3:c.497T>G NP_068745.2:p.Leu166Ter
XM_011520264.1:c.497T>G XP_011518566.1:p.Leu166Ter
XM_011520265.1:c.-26T>G XP_011518567.1:n.-26T>G
XM_011520266.1:c.-26T>G XP_011518568.1:n.-26T>G
NM_021926.4:c.497T>G MANE Select NP_068745.2:p.Leu166Ter
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