Canonical Allele Identifier: CA395997814

Gene: SLC12A3

Linked Data

• MyVariant Identifiers: chr16:g.56928553G>C (hg19) ; chr16:g.56894641G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56894641G>C , CM000678.2:g.56894641G>C	GRCh38
NC_000016.9:g.56928553G>C , CM000678.1:g.56928553G>C	GRCh37
NC_000016.8:g.55486054G>C	NCBI36
NG_009386.1:g.34435G>C
NG_009386.2:g.34435G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2632G>C MANE Select	ENSP00000456149.2:p.Ala878Pro
ENST00000262502.5:c.2629G>C	ENSP00000262502.5:p.Ala877Pro
ENST00000438926.6:c.2659G>C	ENSP00000402152.2:p.Ala887Pro
ENST00000563236.5:c.2632G>C	ENSP00000456149.1:p.Ala878Pro
ENST00000566786.5:c.2656G>C	ENSP00000457552.1:p.Ala886Pro
NM_000339.2:c.2659G>C	NP_000330.2:p.Ala887Pro
NM_001126107.1:c.2656G>C	NP_001119579.1:p.Ala886Pro
NM_001126108.1:c.2632G>C	NP_001119580.1:p.Ala878Pro
XM_005256119.1:c.2629G>C	XP_005256176.1:p.Ala877Pro
XM_005256119.2:c.2629G>C	XP_005256176.1:p.Ala877Pro
NM_000339.3:c.2659G>C	NP_000330.3:p.Ala887Pro
NM_001126107.2:c.2656G>C	NP_001119579.2:p.Ala886Pro
NM_001126108.2:c.2632G>C MANE Select	NP_001119580.2:p.Ala878Pro