Canonical Allele Identifier: CA395997445

Gene: SLC12A3

Linked Data

• MyVariant Identifiers: chr16:g.56928491G>C (hg19) ; chr16:g.56894579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56894579G>C , CM000678.2:g.56894579G>C	GRCh38
NC_000016.9:g.56928491G>C , CM000678.1:g.56928491G>C	GRCh37
NC_000016.8:g.55485992G>C	NCBI36
NG_009386.1:g.34373G>C
NG_009386.2:g.34373G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2570G>C MANE Select	ENSP00000456149.2:p.Ser857Thr
ENST00000262502.5:c.2567G>C	ENSP00000262502.5:p.Ser856Thr
ENST00000438926.6:c.2597G>C	ENSP00000402152.2:p.Ser866Thr
ENST00000563236.5:c.2570G>C	ENSP00000456149.1:p.Ser857Thr
ENST00000566786.5:c.2594G>C	ENSP00000457552.1:p.Ser865Thr
NM_000339.2:c.2597G>C	NP_000330.2:p.Ser866Thr
NM_001126107.1:c.2594G>C	NP_001119579.1:p.Ser865Thr
NM_001126108.1:c.2570G>C	NP_001119580.1:p.Ser857Thr
XM_005256119.1:c.2567G>C	XP_005256176.1:p.Ser856Thr
XM_005256119.2:c.2567G>C	XP_005256176.1:p.Ser856Thr
NM_000339.3:c.2597G>C	NP_000330.3:p.Ser866Thr
NM_001126107.2:c.2594G>C	NP_001119579.2:p.Ser865Thr
NM_001126108.2:c.2570G>C MANE Select	NP_001119580.2:p.Ser857Thr