Canonical Allele Identifier: CA2224357157

Gene: SLC12A3

Linked Data

• dbSNP Id: rs2055309479
• gnomAD v4: 16-56886311-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56886316del , CM000678.2:g.56886316del	GRCh38
NC_000016.9:g.56920228del , CM000678.1:g.56920228del	GRCh37
NC_000016.8:g.55477729del	NCBI36
NG_009386.1:g.26110del
NG_009386.2:g.26110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.1926-48del MANE Select	ENSP00000456149.2:n.1926-48del
ENST00000262502.5:c.1923-48del	ENSP00000262502.5:n.1923-48del
ENST00000438926.6:c.1926-48del	ENSP00000402152.2:n.1926-48del
ENST00000563236.5:c.1926-48del	ENSP00000456149.1:n.1926-48del
ENST00000566786.5:c.1923-48del	ENSP00000457552.1:n.1923-48del
NM_000339.2:c.1926-48del	NP_000330.2:n.1926-48del
NM_001126107.1:c.1923-48del	NP_001119579.1:n.1923-48del
NM_001126108.1:c.1926-48del	NP_001119580.1:n.1926-48del
XM_005256119.1:c.1923-48del	XP_005256176.1:n.1923-48del
XM_005256119.2:c.1923-48del	XP_005256176.1:n.1923-48del
NM_000339.3:c.1926-48del	NP_000330.3:n.1926-48del
NM_001126107.2:c.1923-48del	NP_001119579.2:n.1923-48del
NM_001126108.2:c.1926-48del MANE Select	NP_001119580.2:n.1926-48del