Canonical Allele Identifier: CA2071402480

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128815131A= , CM000674.2:g.128815131A=	GRCh38
NC_000012.11:g.129299676A= , CM000674.1:g.129299676A=	GRCh37
NC_000012.10:g.127865629A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.547-61T= MANE Select	ENSP00000266771.5:n.547-61T=
ENST00000266771.9:c.547-61T=	ENSP00000266771.5:n.547-61T=
ENST00000366292.6:n.798T=
ENST00000376740.8:c.126-61T=
ENST00000376744.8:c.383-61T=
ENST00000535272.1:n.341-61T=
ENST00000539703.1:n.197-61T=
NM_145648.3:c.547-61T=	NP_663623.1:n.547-61T=
XM_011537895.1:c.697-61T=	XP_011536197.1:n.697-61T=
XR_429081.2:n.570-61T=
XR_944494.1:n.720-61T=
XR_944495.1:n.720-61T=
XR_944496.1:n.720-61T=
XR_944497.1:n.720-61T=
XM_017018791.1:c.697-61T=	XP_016874280.1:n.697-61T=
XM_017018792.1:c.697-61T=	XP_016874281.1:n.697-61T=
XM_017018793.1:c.547-61T=	XP_016874282.1:n.547-61T=
XR_002957287.1:n.570-61T=
XR_944496.2:n.720-61T=
NM_145648.4:c.547-61T= MANE Select	NP_663623.1:n.547-61T=