Canonical Allele Identifier: CA953192165
Gene: SLC15A4 HGNC NCBI

Linked Data

dbSNP Id: rs1955733641

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.128815118_128815133del , CM000674.2:g.128815118_128815133del GRCh38
NC_000012.11:g.129299663_129299678del , CM000674.1:g.129299663_129299678del GRCh37
NC_000012.10:g.127865616_127865631del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266771.10:c.547-63_547-48del MANE Select ENSP00000266771.5:n.547-63_547-48del
ENST00000266771.9:c.547-63_547-48del ENSP00000266771.5:n.547-63_547-48del
ENST00000366292.6:n.796_811del
ENST00000376740.8:c.126-63_126-48del
ENST00000376744.8:c.383-63_383-48del
ENST00000535272.1:n.341-63_341-48del
ENST00000539703.1:n.197-63_197-48del
NM_145648.3:c.547-63_547-48del NP_663623.1:n.547-63_547-48del
XM_011537895.1:c.697-63_697-48del XP_011536197.1:n.697-63_697-48del
XR_429081.2:n.570-63_570-48del
XR_944494.1:n.720-63_720-48del
XR_944495.1:n.720-63_720-48del
XR_944496.1:n.720-63_720-48del
XR_944497.1:n.720-63_720-48del
XM_017018791.1:c.697-63_697-48del XP_016874280.1:n.697-63_697-48del
XM_017018792.1:c.697-63_697-48del XP_016874281.1:n.697-63_697-48del
XM_017018793.1:c.547-63_547-48del XP_016874282.1:n.547-63_547-48del
XR_002957287.1:n.570-63_570-48del
XR_944496.2:n.720-63_720-48del
NM_145648.4:c.547-63_547-48del MANE Select NP_663623.1:n.547-63_547-48del