Canonical Allele Identifier: CA495603796

Gene: SLC12A3

Linked Data

• MyVariant Identifiers: chr16:g.56913495T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56879583T>G , CM000678.2:g.56879583T>G	GRCh38
NC_000016.9:g.56913495T>G , CM000678.1:g.56913495T>G	GRCh37
NC_000016.8:g.55470996T>G	NCBI36
NG_009386.1:g.19377T>G
NG_009386.2:g.19377T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.1377T>G MANE Select	ENSP00000456149.2:p.Ala459=
ENST00000262502.5:c.1374T>G	ENSP00000262502.5:p.Ala458=
ENST00000438926.6:c.1377T>G	ENSP00000402152.2:p.Ala459=
ENST00000563236.5:c.1377T>G	ENSP00000456149.1:p.Ala459=
ENST00000566786.5:c.1374T>G	ENSP00000457552.1:p.Ala458=
NM_000339.2:c.1377T>G	NP_000330.2:p.Ala459=
NM_001126107.1:c.1374T>G	NP_001119579.1:p.Ala458=
NM_001126108.1:c.1377T>G	NP_001119580.1:p.Ala459=
XM_005256119.1:c.1374T>G	XP_005256176.1:p.Ala458=
XM_005256119.2:c.1374T>G	XP_005256176.1:p.Ala458=
NM_000339.3:c.1377T>G	NP_000330.3:p.Ala459=
NM_001126107.2:c.1374T>G	NP_001119579.2:p.Ala458=
NM_001126108.2:c.1377T>G MANE Select	NP_001119580.2:p.Ala459=