Canonical Allele Identifier: CA281520937

Gene: SLC12A3

Linked Data

• dbSNP Id: rs372858327

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904098_56904104dup , CM000678.2:g.56904098_56904104dup	GRCh38
NC_000016.9:g.56938010_56938016dup , CM000678.1:g.56938010_56938016dup	GRCh37
NC_000016.8:g.55495511_55495517dup	NCBI36
NG_009386.1:g.43892_43898dup
NG_009386.2:g.43892_43898dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2857-297_2857-291dup MANE Select	ENSP00000456149.2:n.2857-297_2857-291dup
ENST00000262502.5:c.2854-297_2854-291dup	ENSP00000262502.5:n.2854-297_2854-291dup
ENST00000438926.6:c.2884-297_2884-291dup	ENSP00000402152.2:n.2884-297_2884-291dup
ENST00000563236.5:c.2857-297_2857-291dup	ENSP00000456149.1:n.2857-297_2857-291dup
ENST00000566786.5:c.2881-297_2881-291dup	ENSP00000457552.1:n.2881-297_2881-291dup
ENST00000569002.1:n.288-297_288-291dup
NM_000339.2:c.2884-297_2884-291dup	NP_000330.2:n.2884-297_2884-291dup
NM_001126107.1:c.2881-297_2881-291dup	NP_001119579.1:n.2881-297_2881-291dup
NM_001126108.1:c.2857-297_2857-291dup	NP_001119580.1:n.2857-297_2857-291dup
XM_005256119.1:c.2854-297_2854-291dup	XP_005256176.1:n.2854-297_2854-291dup
XM_005256119.2:c.2854-297_2854-291dup	XP_005256176.1:n.2854-297_2854-291dup
NM_000339.3:c.2884-297_2884-291dup	NP_000330.3:n.2884-297_2884-291dup
NM_001126107.2:c.2881-297_2881-291dup	NP_001119579.2:n.2881-297_2881-291dup
NM_001126108.2:c.2857-297_2857-291dup MANE Select	NP_001119580.2:n.2857-297_2857-291dup