Canonical Allele Identifier: CA775650128

Gene: SLC38A10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81288009C>T , CM000679.2:g.81288009C>T	GRCh38
NC_000017.10:g.79261809C>T , CM000679.1:g.79261809C>T	GRCh37
NC_000017.9:g.76876404C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374759.8:c.217+1682G>A MANE Select	ENSP00000363891.3:n.217+1682G>A
ENST00000288439.9:c.217+1682G>A	ENSP00000288439.5:n.217+1682G>A
ENST00000374759.7:c.217+1682G>A	ENSP00000363891.3:n.217+1682G>A
ENST00000539748.1:c.73+1682G>A	ENSP00000439115.1:n.73+1682G>A
NM_001037984.2:c.217+1682G>A	NP_001033073.1:n.217+1682G>A
NM_138570.3:c.217+1682G>A	NP_612637.1:n.217+1682G>A
XM_005257019.1:c.217+1682G>A	XP_005257076.1:n.217+1682G>A
XM_011524288.1:c.238+1661G>A	XP_011522590.1:n.238+1661G>A
XM_011524289.1:c.238+1661G>A	XP_011522591.1:n.238+1661G>A
NM_001037984.3:c.217+1682G>A MANE Select	NP_001033073.1:n.217+1682G>A
NM_138570.4:c.217+1682G>A	NP_612637.1:n.217+1682G>A