Canonical Allele Identifier: CA2621852376
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128814693_128814719dup , CM000674.2:g.128814693_128814719dup GRCh38
NC_000012.11:g.129299238_129299264dup , CM000674.1:g.129299238_129299264dup GRCh37
NC_000012.10:g.127865191_127865217dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.842+57_842+83dup MANE Select ENSP00000266771.5:n.842+57_842+83dup
ENST00000266771.9:c.842+57_842+83dup ENSP00000266771.5:n.842+57_842+83dup
ENST00000366292.6:n.1154+57_1154+83dup
ENST00000376740.8:c.421+57_421+83dup
ENST00000376744.8:c.678+57_678+83dup
ENST00000539703.1:n.492+57_492+83dup
ENST00000614634.1:c.-1+57_-1+83dup ENSP00000483143.1:n.-1+57_-1+83dup
NM_145648.3:c.842+57_842+83dup NP_663623.1:n.842+57_842+83dup
XM_011537895.1:c.992+57_992+83dup XP_011536197.1:n.992+57_992+83dup
XR_429081.2:n.865+57_865+83dup
XR_944494.1:n.1015+57_1015+83dup
XR_944495.1:n.1015+57_1015+83dup
XR_944496.1:n.1015+57_1015+83dup
XR_944497.1:n.1015+57_1015+83dup
XM_017018791.1:c.992+57_992+83dup XP_016874280.1:n.992+57_992+83dup
XM_017018792.1:c.992+57_992+83dup XP_016874281.1:n.992+57_992+83dup
XM_017018793.1:c.842+57_842+83dup XP_016874282.1:n.842+57_842+83dup
XR_002957287.1:n.865+57_865+83dup
XR_944496.2:n.1015+57_1015+83dup
NM_145648.4:c.842+57_842+83dup MANE Select NP_663623.1:n.842+57_842+83dup