Canonical Allele Identifier: CA2224356236

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56884375T= , CM000678.2:g.56884375T=	GRCh38
NC_000016.9:g.56918287T= , CM000678.1:g.56918287T=	GRCh37
NC_000016.8:g.55475788T=	NCBI36
NG_009386.1:g.24169T=
NG_009386.2:g.24169T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.1825+171T= MANE Select	ENSP00000456149.2:n.1825+171T=
ENST00000262502.5:c.1822+171T=	ENSP00000262502.5:n.1822+171T=
ENST00000438926.6:c.1825+171T=	ENSP00000402152.2:n.1825+171T=
ENST00000563236.5:c.1825+171T=	ENSP00000456149.1:n.1825+171T=
ENST00000566786.5:c.1822+171T=	ENSP00000457552.1:n.1822+171T=
NM_000339.2:c.1825+171T=	NP_000330.2:n.1825+171T=
NM_001126107.1:c.1822+171T=	NP_001119579.1:n.1822+171T=
NM_001126108.1:c.1825+171T=	NP_001119580.1:n.1825+171T=
XM_005256119.1:c.1822+171T=	XP_005256176.1:n.1822+171T=
XM_005256119.2:c.1822+171T=	XP_005256176.1:n.1822+171T=
NM_000339.3:c.1825+171T=	NP_000330.3:n.1825+171T=
NM_001126107.2:c.1822+171T=	NP_001119579.2:n.1822+171T=
NM_001126108.2:c.1825+171T= MANE Select	NP_001119580.2:n.1825+171T=