Canonical Allele Identifier: CA281492942

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56867068A>C , CM000678.2:g.56867068A>C	GRCh38
NC_000016.9:g.56900980A>C , CM000678.1:g.56900980A>C	GRCh37
NC_000016.8:g.55458481A>C	NCBI36
NG_009386.1:g.6862A>C
NG_009386.2:g.6862A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001126108.2:c.283-2A>C MANE Select	NP_001119580.2:n.283-2A>C
ENST00000563236.6:c.283-2A>C MANE Select	ENSP00000456149.2:n.283-2A>C
NM_000339.2:c.283-2A>C	NP_000330.2:n.283-2A>C
NM_000339.3:c.283-2A>C	NP_000330.3:n.283-2A>C
NM_001126107.1:c.283-5A>C	NP_001119579.1:n.283-5A>C
NM_001126107.2:c.283-5A>C	NP_001119579.2:n.283-5A>C
NM_001126108.1:c.283-2A>C	NP_001119580.1:n.283-2A>C
ENST00000262502.5:c.283-5A>C	ENSP00000262502.5:n.283-5A>C
ENST00000438926.6:c.283-2A>C	ENSP00000402152.2:n.283-2A>C
ENST00000563236.5:c.283-2A>C	ENSP00000456149.1:n.283-2A>C
ENST00000566786.5:c.283-5A>C	ENSP00000457552.1:n.283-5A>C
XM_005256119.1:c.283-5A>C	XP_005256176.1:n.283-5A>C
XM_005256119.2:c.283-5A>C	XP_005256176.1:n.283-5A>C