Canonical Allele Identifier: CA919713951

Gene: SLC12A3

Linked Data

• dbSNP Id: rs1555502381

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56902779dup , CM000678.2:g.56902779dup	GRCh38
NC_000016.9:g.56936691dup , CM000678.1:g.56936691dup	GRCh37
NC_000016.8:g.55494192dup	NCBI36
NG_009386.1:g.42573dup
NG_009386.2:g.42573dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2856+271dup MANE Select	ENSP00000456149.2:n.2856+271dup
ENST00000262502.5:c.2853+271dup	ENSP00000262502.5:n.2853+271dup
ENST00000438926.6:c.2883+271dup	ENSP00000402152.2:n.2883+271dup
ENST00000563236.5:c.2856+271dup	ENSP00000456149.1:n.2856+271dup
ENST00000566786.5:c.2880+271dup	ENSP00000457552.1:n.2880+271dup
ENST00000569002.1:n.287+271dup
NM_000339.2:c.2883+271dup	NP_000330.2:n.2883+271dup
NM_001126107.1:c.2880+271dup	NP_001119579.1:n.2880+271dup
NM_001126108.1:c.2856+271dup	NP_001119580.1:n.2856+271dup
XM_005256119.1:c.2853+271dup	XP_005256176.1:n.2853+271dup
XM_005256119.2:c.2853+271dup	XP_005256176.1:n.2853+271dup
NM_000339.3:c.2883+271dup	NP_000330.3:n.2883+271dup
NM_001126107.2:c.2880+271dup	NP_001119579.2:n.2880+271dup
NM_001126108.2:c.2856+271dup MANE Select	NP_001119580.2:n.2856+271dup