Canonical Allele Identifier: CA392307065

Gene: SLC12A1

Linked Data

• MyVariant Identifiers: chr15:g.48521467C>T (hg19) ; chr15:g.48229270C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48229270C>T , CM000677.2:g.48229270C>T	GRCh38
NC_000015.9:g.48521467C>T , CM000677.1:g.48521467C>T	GRCh37
NC_000015.8:g.46308759C>T	NCBI36
NG_021301.1:g.27970C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686073.1:c.806C>T	ENSP00000508901.1:p.Ala269Val
ENST00000380993.8:c.806C>T MANE Select	ENSP00000370381.3:p.Ala269Val
ENST00000646012.1:c.944C>T	ENSP00000495813.1:p.Ala315Val
ENST00000647232.1:c.806C>T	ENSP00000493875.1:p.Ala269Val
ENST00000647546.1:c.806C>T	ENSP00000495332.1:p.Ala269Val
ENST00000330289.10:c.806C>T	ENSP00000331550.6:p.Ala269Val
ENST00000380993.7:c.806C>T	ENSP00000370381.3:p.Ala269Val
ENST00000396577.7:c.806C>T	ENSP00000379822.3:p.Ala269Val
ENST00000558252.5:n.4929C>T
ENST00000558405.5:c.806C>T	ENSP00000453409.1:p.Ala269Val
ENST00000559641.5:c.245C>T	ENSP00000453230.1:p.Ala82Val
ENST00000559723.2:n.179C>T
ENST00000560692.5:n.4945C>T
ENST00000561127.5:c.245C>T	ENSP00000453602.2:p.Ala82Val
NM_000338.2:c.806C>T	NP_000329.2:p.Ala269Val
NM_001184832.1:c.806C>T	NP_001171761.1:p.Ala269Val
XM_005254605.1:c.902C>T	XP_005254662.1:p.Ala301Val
XM_005254606.1:c.806C>T	XP_005254663.1:p.Ala269Val
XM_006720656.1:c.902C>T	XP_006720719.1:p.Ala301Val
XR_931896.1:n.1118C>T
XR_932203.1:n.229+686G>A
XR_932204.1:n.222+686G>A
XM_005254606.2:c.806C>T	XP_005254663.1:p.Ala269Val
XR_001751524.2:n.230+686G>A
XR_001751525.1:n.230+686G>A
XR_002957762.1:n.230+686G>A
XR_932204.3:n.224+686G>A
NM_000338.3:c.806C>T MANE Select	NP_000329.2:p.Ala269Val
NM_001184832.2:c.806C>T	NP_001171761.1:p.Ala269Val
NM_001384136.1:c.806C>T	NP_001371065.1:p.Ala269Val