Canonical Allele Identifier: CA396002313

Gene: SLC12A3

Linked Data

• MyVariant Identifiers: chr16:g.56938328A>G (hg19) ; chr16:g.56904416A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904416A>G , CM000678.2:g.56904416A>G	GRCh38
NC_000016.9:g.56938328A>G , CM000678.1:g.56938328A>G	GRCh37
NC_000016.8:g.55495829A>G	NCBI36
NG_009386.1:g.44210A>G
NG_009386.2:g.44210A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000563236.6:c.2878A>G MANE Select	ENSP00000456149.2:p.Asn960Asp
ENST00000262502.5:c.2875A>G	ENSP00000262502.5:p.Asn959Asp
ENST00000438926.6:c.2905A>G	ENSP00000402152.2:p.Asn969Asp
ENST00000563236.5:c.2878A>G	ENSP00000456149.1:p.Asn960Asp
ENST00000566786.5:c.2902A>G	ENSP00000457552.1:p.Asn968Asp
ENST00000569002.1:n.309A>G
NM_000339.2:c.2905A>G	NP_000330.2:p.Asn969Asp
NM_001126107.1:c.2902A>G	NP_001119579.1:p.Asn968Asp
NM_001126108.1:c.2878A>G	NP_001119580.1:p.Asn960Asp
XM_005256119.1:c.2875A>G	XP_005256176.1:p.Asn959Asp
XM_005256119.2:c.2875A>G	XP_005256176.1:p.Asn959Asp
NM_000339.3:c.2905A>G	NP_000330.3:p.Asn969Asp
NM_001126107.2:c.2902A>G	NP_001119579.2:p.Asn968Asp
NM_001126108.2:c.2878A>G MANE Select	NP_001119580.2:p.Asn960Asp