Canonical Allele Identifier: CA953192163

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1955733568
• gnomAD v3: 12-128815114-CTT-C
• gnomAD v4: 12-128815114-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815115_128815116del , CM000674.2:g.128815115_128815116del	GRCh38
NC_000012.11:g.129299660_129299661del , CM000674.1:g.129299660_129299661del	GRCh37
NC_000012.10:g.127865613_127865614del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-46_547-45del MANE Select	ENSP00000266771.5:n.547-46_547-45del
ENST00000266771.9:c.547-46_547-45del	ENSP00000266771.5:n.547-46_547-45del
ENST00000366292.6:n.813_814del
ENST00000376740.8:c.126-46_126-45del
ENST00000376744.8:c.383-46_383-45del
ENST00000535272.1:n.341-46_341-45del
ENST00000539703.1:n.197-46_197-45del
NM_145648.3:c.547-46_547-45del	NP_663623.1:n.547-46_547-45del
XM_011537895.1:c.697-46_697-45del	XP_011536197.1:n.697-46_697-45del
XR_429081.2:n.570-46_570-45del
XR_944494.1:n.720-46_720-45del
XR_944495.1:n.720-46_720-45del
XR_944496.1:n.720-46_720-45del
XR_944497.1:n.720-46_720-45del
XM_017018791.1:c.697-46_697-45del	XP_016874280.1:n.697-46_697-45del
XM_017018792.1:c.697-46_697-45del	XP_016874281.1:n.697-46_697-45del
XM_017018793.1:c.547-46_547-45del	XP_016874282.1:n.547-46_547-45del
XR_002957287.1:n.570-46_570-45del
XR_944496.2:n.720-46_720-45del
NM_145648.4:c.547-46_547-45del MANE Select	NP_663623.1:n.547-46_547-45del