Canonical Allele Identifier: CA2224357266

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56886512_56886513delinsTG , CM000678.2:g.56886512_56886513delinsTG	GRCh38
NC_000016.9:g.56920424_56920425delinsTG , CM000678.1:g.56920424_56920425delinsTG	GRCh37
NC_000016.8:g.55477925_55477926delinsTG	NCBI36
NG_009386.1:g.26306_26307delinsTG
NG_009386.2:g.26306_26307delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2037+37_2037+38delinsTG MANE Select	ENSP00000456149.2:n.2037+37_2037+38delinsTG
ENST00000262502.5:c.2034+37_2034+38delinsTG	ENSP00000262502.5:n.2034+37_2034+38delinsTG
ENST00000438926.6:c.2037+37_2037+38delinsTG	ENSP00000402152.2:n.2037+37_2037+38delinsTG
ENST00000563236.5:c.2037+37_2037+38delinsTG	ENSP00000456149.1:n.2037+37_2037+38delinsTG
ENST00000566786.5:c.2034+37_2034+38delinsTG	ENSP00000457552.1:n.2034+37_2034+38delinsTG
NM_000339.2:c.2037+37_2037+38delinsTG	NP_000330.2:n.2037+37_2037+38delinsTG
NM_001126107.1:c.2034+37_2034+38delinsTG	NP_001119579.1:n.2034+37_2034+38delinsTG
NM_001126108.1:c.2037+37_2037+38delinsTG	NP_001119580.1:n.2037+37_2037+38delinsTG
XM_005256119.1:c.2034+37_2034+38delinsTG	XP_005256176.1:n.2034+37_2034+38delinsTG
XM_005256119.2:c.2034+37_2034+38delinsTG	XP_005256176.1:n.2034+37_2034+38delinsTG
NM_000339.3:c.2037+37_2037+38delinsTG	NP_000330.3:n.2037+37_2037+38delinsTG
NM_001126107.2:c.2034+37_2034+38delinsTG	NP_001119579.2:n.2034+37_2034+38delinsTG
NM_001126108.2:c.2037+37_2037+38delinsTG MANE Select	NP_001119580.2:n.2037+37_2037+38delinsTG