Canonical Allele Identifier: CA1591323542

Gene: SLC36A3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151279478A= , CM000667.2:g.151279478A=	GRCh38
NC_000005.9:g.150659039A= , CM000667.1:g.150659039A=	GRCh37
NC_000005.8:g.150639232A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000335230.8:c.1144+1536T= MANE Select	ENSP00000334750.3:n.1144+1536T=
ENST00000335230.7:c.1144+1536T=	ENSP00000334750.3:n.1144+1536T=
ENST00000377713.3:c.1267+1536T=	ENSP00000366942.3:n.1267+1536T=
ENST00000423071.2:n.3044+1536T=
NM_001145017.1:c.1267+1536T=	NP_001138489.1:n.1267+1536T=
NM_181774.3:c.1144+1536T=	NP_861439.3:n.1144+1536T=
XM_006714781.1:c.995-1817T=	XP_006714844.1:n.995-1817T=
XM_011537626.1:c.1138+1536T=	XP_011535928.1:n.1138+1536T=
XM_011537627.1:c.1066+1536T=	XP_011535929.1:n.1066+1536T=
XM_011537628.1:c.1000+1536T=	XP_011535930.1:n.1000+1536T=
XM_011537629.1:c.975-1817T=	XP_011535931.1:n.975-1817T=
XM_011537630.1:c.799+1536T=	XP_011535932.1:n.799+1536T=
XM_011537631.1:c.799+1536T=	XP_011535933.1:n.799+1536T=
XM_011537632.1:c.799+1536T=	XP_011535934.1:n.799+1536T=
XM_011537633.1:c.655+1536T=	XP_011535935.1:n.655+1536T=
XR_427775.1:n.1592+1536T=
XM_011537627.3:c.1066+1536T=	XP_011535929.1:n.1066+1536T=
XM_011537629.3:c.975-1817T=	XP_011535931.1:n.975-1817T=
XM_011537630.2:c.799+1536T=	XP_011535932.1:n.799+1536T=
XM_011537631.2:c.799+1536T=	XP_011535933.1:n.799+1536T=
XR_427775.3:n.1576+1536T=
NM_001145017.2:c.1267+1536T=	NP_001138489.1:n.1267+1536T=
NM_181774.4:c.1144+1536T= MANE Select	NP_861439.3:n.1144+1536T=