Canonical Allele Identifier: CA380182722
Gene: ALX4 HGNC NCBI

Linked Data

dbSNP Id: rs1458347692

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44275626G>A , CM000673.2:g.44275626G>A GRCh38
NC_000011.9:g.44297176G>A , CM000673.1:g.44297176G>A GRCh37
NC_000011.8:g.44253752G>A NCBI36
NG_015809.1:g.39541C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000652299.1:c.499C>T MANE Select ENSP00000498217.1:p.Pro167Ser
ENST00000329255.3:c.499C>T ENSP00000332744.3:p.Pro167Ser
NM_021926.3:c.499C>T NP_068745.2:p.Pro167Ser
XM_011520264.1:c.499C>T XP_011518566.1:p.Pro167Ser
XM_011520265.1:c.-24C>T XP_011518567.1:n.-24C>T
XM_011520266.1:c.-24C>T XP_011518568.1:n.-24C>T
NM_021926.4:c.499C>T MANE Select NP_068745.2:p.Pro167Ser