Canonical Allele Identifier: CA2071401132

Gene: SLC15A4

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.128814367G= , CM000674.2:g.128814367G=	GRCh38
NC_000012.11:g.129298912G= , CM000674.1:g.129298912G=	GRCh37
NC_000012.10:g.127864865G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266771.10:c.842+408C= MANE Select	ENSP00000266771.5:n.842+408C=
ENST00000266771.9:c.842+408C=	ENSP00000266771.5:n.842+408C=
ENST00000366292.6:n.1154+408C=
ENST00000376740.8:c.421+408C=
ENST00000376744.8:c.678+408C=
ENST00000539703.1:n.492+408C=
ENST00000614634.1:c.-1+408C=	ENSP00000483143.1:n.-1+408C=
NM_145648.3:c.842+408C=	NP_663623.1:n.842+408C=
XM_011537895.1:c.992+408C=	XP_011536197.1:n.992+408C=
XR_429081.2:n.865+408C=
XR_944494.1:n.1015+408C=
XR_944495.1:n.1015+408C=
XR_944496.1:n.1015+408C=
XR_944497.1:n.1015+408C=
XM_017018791.1:c.992+408C=	XP_016874280.1:n.992+408C=
XM_017018792.1:c.992+408C=	XP_016874281.1:n.992+408C=
XM_017018793.1:c.842+408C=	XP_016874282.1:n.842+408C=
XR_002957287.1:n.865+408C=
XR_944496.2:n.1015+408C=
NM_145648.4:c.842+408C= MANE Select	NP_663623.1:n.842+408C=