Canonical Allele Identifier: CA685199383

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1211232783
• gnomAD v3: 12-128815158-GTT-G
• gnomAD v4: 12-128815158-GTT-G
• MyVariant Identifiers: chr12:g.129299704_129299705del (hg19) ; chr12:g.128815159_128815160del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815159_128815160del , CM000674.2:g.128815159_128815160del	GRCh38
NC_000012.11:g.129299704_129299705del , CM000674.1:g.129299704_129299705del	GRCh37
NC_000012.10:g.127865657_127865658del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-90_547-89del MANE Select	ENSP00000266771.5:n.547-90_547-89del
ENST00000266771.9:c.547-90_547-89del	ENSP00000266771.5:n.547-90_547-89del
ENST00000366292.6:n.769_770del
ENST00000376740.8:c.126-90_126-89del
ENST00000376744.8:c.383-90_383-89del
ENST00000535272.1:n.341-90_341-89del
ENST00000539703.1:n.197-90_197-89del
NM_145648.3:c.547-90_547-89del	NP_663623.1:n.547-90_547-89del
XM_011537895.1:c.697-90_697-89del	XP_011536197.1:n.697-90_697-89del
XR_429081.2:n.570-90_570-89del
XR_944494.1:n.720-90_720-89del
XR_944495.1:n.720-90_720-89del
XR_944496.1:n.720-90_720-89del
XR_944497.1:n.720-90_720-89del
XM_017018791.1:c.697-90_697-89del	XP_016874280.1:n.697-90_697-89del
XM_017018792.1:c.697-90_697-89del	XP_016874281.1:n.697-90_697-89del
XM_017018793.1:c.547-90_547-89del	XP_016874282.1:n.547-90_547-89del
XR_002957287.1:n.570-90_570-89del
XR_944496.2:n.720-90_720-89del
NM_145648.4:c.547-90_547-89del MANE Select	NP_663623.1:n.547-90_547-89del