Canonical Allele Identifier: CA2621852426
Gene: SLC15A4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128815093_128815095del , CM000674.2:g.128815093_128815095del GRCh38
NC_000012.11:g.129299638_129299640del , CM000674.1:g.129299638_129299640del GRCh37
NC_000012.10:g.127865591_127865593del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.547-25_547-23del MANE Select ENSP00000266771.5:n.547-25_547-23del
ENST00000266771.9:c.547-25_547-23del ENSP00000266771.5:n.547-25_547-23del
ENST00000366292.6:n.834_836del
ENST00000376740.8:c.126-25_126-23del
ENST00000376744.8:c.383-25_383-23del
ENST00000535272.1:n.341-25_341-23del
ENST00000539703.1:n.197-25_197-23del
NM_145648.3:c.547-25_547-23del NP_663623.1:n.547-25_547-23del
XM_011537895.1:c.697-25_697-23del XP_011536197.1:n.697-25_697-23del
XR_429081.2:n.570-25_570-23del
XR_944494.1:n.720-25_720-23del
XR_944495.1:n.720-25_720-23del
XR_944496.1:n.720-25_720-23del
XR_944497.1:n.720-25_720-23del
XM_017018791.1:c.697-25_697-23del XP_016874280.1:n.697-25_697-23del
XM_017018792.1:c.697-25_697-23del XP_016874281.1:n.697-25_697-23del
XM_017018793.1:c.547-25_547-23del XP_016874282.1:n.547-25_547-23del
XR_002957287.1:n.570-25_570-23del
XR_944496.2:n.720-25_720-23del
NM_145648.4:c.547-25_547-23del MANE Select NP_663623.1:n.547-25_547-23del