Canonical Allele Identifier: CA3222325800

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56913250T= , CM000678.2:g.56913250T=	GRCh38
NC_000016.9:g.56947162T= , CM000678.1:g.56947162T=	GRCh37
NC_000016.8:g.55504663T=	NCBI36
NG_009386.1:g.53044T=
NG_009386.2:g.53044T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001126108.2:c.2925-14T= MANE Select	NP_001119580.2:n.2925-14T=
ENST00000563236.6:c.2925-14T= MANE Select	ENSP00000456149.2:n.2925-14T=
NM_000339.2:c.2952-14T=	NP_000330.2:n.2952-14T=
NM_000339.3:c.2952-14T=	NP_000330.3:n.2952-14T=
NM_001126107.1:c.2949-14T=	NP_001119579.1:n.2949-14T=
NM_001126107.2:c.2949-14T=	NP_001119579.2:n.2949-14T=
NM_001126108.1:c.2925-14T=	NP_001119580.1:n.2925-14T=
ENST00000262502.5:c.2922-14T=	ENSP00000262502.5:n.2922-14T=
ENST00000438926.6:c.2952-14T=	ENSP00000402152.2:n.2952-14T=
ENST00000563236.5:c.2925-14T=	ENSP00000456149.1:n.2925-14T=
ENST00000563352.1:n.73-14T=
ENST00000566786.5:c.2949-14T=	ENSP00000457552.1:n.2949-14T=
XM_005256119.1:c.2922-14T=	XP_005256176.1:n.2922-14T=
XM_005256119.2:c.2922-14T=	XP_005256176.1:n.2922-14T=