Canonical Allele Identifier: CA953192158

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1955733450
• gnomAD v3: 12-128815108-GACAGTCTTCAAGGATGAAA-G
• gnomAD v4: 12-128815108-GACAGTCTTCAAGGATGAAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815111_128815129del , CM000674.2:g.128815111_128815129del	GRCh38
NC_000012.11:g.129299656_129299674del , CM000674.1:g.129299656_129299674del	GRCh37
NC_000012.10:g.127865609_127865627del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-57_547-39del MANE Select	ENSP00000266771.5:n.547-57_547-39del
ENST00000266771.9:c.547-57_547-39del	ENSP00000266771.5:n.547-57_547-39del
ENST00000366292.6:n.802_820del
ENST00000376740.8:c.126-57_126-39del
ENST00000376744.8:c.383-57_383-39del
ENST00000535272.1:n.341-57_341-39del
ENST00000539703.1:n.197-57_197-39del
NM_145648.3:c.547-57_547-39del	NP_663623.1:n.547-57_547-39del
XM_011537895.1:c.697-57_697-39del	XP_011536197.1:n.697-57_697-39del
XR_429081.2:n.570-57_570-39del
XR_944494.1:n.720-57_720-39del
XR_944495.1:n.720-57_720-39del
XR_944496.1:n.720-57_720-39del
XR_944497.1:n.720-57_720-39del
XM_017018791.1:c.697-57_697-39del	XP_016874280.1:n.697-57_697-39del
XM_017018792.1:c.697-57_697-39del	XP_016874281.1:n.697-57_697-39del
XM_017018793.1:c.547-57_547-39del	XP_016874282.1:n.547-57_547-39del
XR_002957287.1:n.570-57_570-39del
XR_944496.2:n.720-57_720-39del
NM_145648.4:c.547-57_547-39del MANE Select	NP_663623.1:n.547-57_547-39del