Canonical Allele Identifier: CA685199333

Gene: SLC15A4

Linked Data

• dbSNP Id: rs1390084582
• MyVariant Identifiers: chr12:g.129299660_129299677del (hg19) ; chr12:g.128815115_128815132del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815115_128815132del , CM000674.2:g.128815115_128815132del	GRCh38
NC_000012.11:g.129299660_129299677del , CM000674.1:g.129299660_129299677del	GRCh37
NC_000012.10:g.127865613_127865630del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-62_547-45del MANE Select	ENSP00000266771.5:n.547-62_547-45del
ENST00000266771.9:c.547-62_547-45del	ENSP00000266771.5:n.547-62_547-45del
ENST00000366292.6:n.797_814del
ENST00000376740.8:c.126-62_126-45del
ENST00000376744.8:c.383-62_383-45del
ENST00000535272.1:n.341-62_341-45del
ENST00000539703.1:n.197-62_197-45del
NM_145648.3:c.547-62_547-45del	NP_663623.1:n.547-62_547-45del
XM_011537895.1:c.697-62_697-45del	XP_011536197.1:n.697-62_697-45del
XR_429081.2:n.570-62_570-45del
XR_944494.1:n.720-62_720-45del
XR_944495.1:n.720-62_720-45del
XR_944496.1:n.720-62_720-45del
XR_944497.1:n.720-62_720-45del
XM_017018791.1:c.697-62_697-45del	XP_016874280.1:n.697-62_697-45del
XM_017018792.1:c.697-62_697-45del	XP_016874281.1:n.697-62_697-45del
XM_017018793.1:c.547-62_547-45del	XP_016874282.1:n.547-62_547-45del
XR_002957287.1:n.570-62_570-45del
XR_944496.2:n.720-62_720-45del
NM_145648.4:c.547-62_547-45del MANE Select	NP_663623.1:n.547-62_547-45del