Canonical Allele Identifier: CA953192181

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1955734314
• gnomAD v3: 12-128815165-TCACAACCTTTAAGAAGCGCAA-T
• gnomAD v4: 12-128815165-TCACAACCTTTAAGAAGCGCAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815171_128815191del , CM000674.2:g.128815171_128815191del	GRCh38
NC_000012.11:g.129299716_129299736del , CM000674.1:g.129299716_129299736del	GRCh37
NC_000012.10:g.127865669_127865689del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-116_547-96del MANE Select	ENSP00000266771.5:n.547-116_547-96del
ENST00000266771.9:c.547-116_547-96del	ENSP00000266771.5:n.547-116_547-96del
ENST00000366292.6:n.743_763del
ENST00000376740.8:c.126-116_126-96del
ENST00000376744.8:c.383-116_383-96del
ENST00000535272.1:n.341-116_341-96del
ENST00000539703.1:n.197-116_197-96del
NM_145648.3:c.547-116_547-96del	NP_663623.1:n.547-116_547-96del
XM_011537895.1:c.697-116_697-96del	XP_011536197.1:n.697-116_697-96del
XR_429081.2:n.570-116_570-96del
XR_944494.1:n.720-116_720-96del
XR_944495.1:n.720-116_720-96del
XR_944496.1:n.720-116_720-96del
XR_944497.1:n.720-116_720-96del
XM_017018791.1:c.697-116_697-96del	XP_016874280.1:n.697-116_697-96del
XM_017018792.1:c.697-116_697-96del	XP_016874281.1:n.697-116_697-96del
XM_017018793.1:c.547-116_547-96del	XP_016874282.1:n.547-116_547-96del
XR_002957287.1:n.570-116_570-96del
XR_944496.2:n.720-116_720-96del
NM_145648.4:c.547-116_547-96del MANE Select	NP_663623.1:n.547-116_547-96del