Canonical Allele Identifier: CA392306991

Gene: SLC12A1

Linked Data

• gnomAD v4: 15-48229254-T-G
• MyVariant Identifiers: chr15:g.48521451T>G (hg19) ; chr15:g.48229254T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48229254T>G , CM000677.2:g.48229254T>G	GRCh38
NC_000015.9:g.48521451T>G , CM000677.1:g.48521451T>G	GRCh37
NC_000015.8:g.46308743T>G	NCBI36
NG_021301.1:g.27954T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686073.1:c.790T>G	ENSP00000508901.1:p.Phe264Val
ENST00000380993.8:c.790T>G MANE Select	ENSP00000370381.3:p.Phe264Val
ENST00000646012.1:c.928T>G	ENSP00000495813.1:p.Phe310Val
ENST00000647232.1:c.790T>G	ENSP00000493875.1:p.Phe264Val
ENST00000647546.1:c.790T>G	ENSP00000495332.1:p.Phe264Val
ENST00000330289.10:c.790T>G	ENSP00000331550.6:p.Phe264Val
ENST00000380993.7:c.790T>G	ENSP00000370381.3:p.Phe264Val
ENST00000396577.7:c.790T>G	ENSP00000379822.3:p.Phe264Val
ENST00000558252.5:n.4913T>G
ENST00000558405.5:c.790T>G	ENSP00000453409.1:p.Phe264Val
ENST00000559641.5:c.229T>G	ENSP00000453230.1:p.Phe77Val
ENST00000559723.2:n.163T>G
ENST00000560692.5:n.4929T>G
ENST00000561127.5:c.229T>G	ENSP00000453602.2:p.Phe77Val
NM_000338.2:c.790T>G	NP_000329.2:p.Phe264Val
NM_001184832.1:c.790T>G	NP_001171761.1:p.Phe264Val
XM_005254605.1:c.886T>G	XP_005254662.1:p.Phe296Val
XM_005254606.1:c.790T>G	XP_005254663.1:p.Phe264Val
XM_006720656.1:c.886T>G	XP_006720719.1:p.Phe296Val
XR_931896.1:n.1102T>G
XR_932203.1:n.229+702A>C
XR_932204.1:n.222+702A>C
XM_005254606.2:c.790T>G	XP_005254663.1:p.Phe264Val
XR_001751524.2:n.230+702A>C
XR_001751525.1:n.230+702A>C
XR_002957762.1:n.230+702A>C
XR_932204.3:n.224+702A>C
NM_000338.3:c.790T>G MANE Select	NP_000329.2:p.Phe264Val
NM_001184832.2:c.790T>G	NP_001171761.1:p.Phe264Val
NM_001384136.1:c.790T>G	NP_001371065.1:p.Phe264Val