Canonical Allele Identifier: CA805666218

Gene: SLC36A3

Linked Data

• dbSNP Id: rs1384245329
• MyVariant Identifiers: chr5:g.150658888T>C (hg19) ; chr5:g.151279327T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.151279327T>C , CM000667.2:g.151279327T>C	GRCh38
NC_000005.9:g.150658888T>C , CM000667.1:g.150658888T>C	GRCh37
NC_000005.8:g.150639081T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335230.8:c.1145-1666A>G MANE Select	ENSP00000334750.3:n.1145-1666A>G
ENST00000335230.7:c.1145-1666A>G	ENSP00000334750.3:n.1145-1666A>G
ENST00000377713.3:c.1268-1666A>G	ENSP00000366942.3:n.1268-1666A>G
ENST00000423071.2:n.3045-1666A>G
NM_001145017.1:c.1268-1666A>G	NP_001138489.1:n.1268-1666A>G
NM_181774.3:c.1145-1666A>G	NP_861439.3:n.1145-1666A>G
XM_006714781.1:c.995-1666A>G	XP_006714844.1:n.995-1666A>G
XM_011537626.1:c.1139-1666A>G	XP_011535928.1:n.1139-1666A>G
XM_011537627.1:c.1067-1666A>G	XP_011535929.1:n.1067-1666A>G
XM_011537628.1:c.1001-1666A>G	XP_011535930.1:n.1001-1666A>G
XM_011537629.1:c.975-1666A>G	XP_011535931.1:n.975-1666A>G
XM_011537630.1:c.800-1666A>G	XP_011535932.1:n.800-1666A>G
XM_011537631.1:c.800-1666A>G	XP_011535933.1:n.800-1666A>G
XM_011537632.1:c.800-1666A>G	XP_011535934.1:n.800-1666A>G
XM_011537633.1:c.656-1666A>G	XP_011535935.1:n.656-1666A>G
XR_427775.1:n.1593-1666A>G
XM_011537627.3:c.1067-1666A>G	XP_011535929.1:n.1067-1666A>G
XM_011537629.3:c.975-1666A>G	XP_011535931.1:n.975-1666A>G
XM_011537630.2:c.800-1666A>G	XP_011535932.1:n.800-1666A>G
XM_011537631.2:c.800-1666A>G	XP_011535933.1:n.800-1666A>G
XR_427775.3:n.1577-1666A>G
NM_001145017.2:c.1268-1666A>G	NP_001138489.1:n.1268-1666A>G
NM_181774.4:c.1145-1666A>G MANE Select	NP_861439.3:n.1145-1666A>G