Canonical Allele Identifier: CA392306760

Gene: SLC12A1

Linked Data

• gnomAD v4: 15-48229188-G-T
• MyVariant Identifiers: chr15:g.48521385G>T (hg19) ; chr15:g.48229188G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48229188G>T , CM000677.2:g.48229188G>T	GRCh38
NC_000015.9:g.48521385G>T , CM000677.1:g.48521385G>T	GRCh37
NC_000015.8:g.46308677G>T	NCBI36
NG_021301.1:g.27888G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686073.1:c.725-1G>T	ENSP00000508901.1:n.725-1G>T
ENST00000380993.8:c.725-1G>T MANE Select	ENSP00000370381.3:n.725-1G>T
ENST00000646012.1:c.863-1G>T	ENSP00000495813.1:n.863-1G>T
ENST00000647232.1:c.725-1G>T	ENSP00000493875.1:n.725-1G>T
ENST00000647546.1:c.725-1G>T	ENSP00000495332.1:n.725-1G>T
ENST00000330289.10:c.725-1G>T	ENSP00000331550.6:n.725-1G>T
ENST00000380993.7:c.725-1G>T	ENSP00000370381.3:n.725-1G>T
ENST00000396577.7:c.725-1G>T	ENSP00000379822.3:n.725-1G>T
ENST00000558252.5:n.4848-1G>T
ENST00000558405.5:c.725-1G>T	ENSP00000453409.1:n.725-1G>T
ENST00000559641.5:c.164-1G>T	ENSP00000453230.1:n.164-1G>T
ENST00000559723.2:n.98-1G>T
ENST00000560692.5:n.4863G>T
ENST00000561127.5:c.164-1G>T	ENSP00000453602.2:n.164-1G>T
NM_000338.2:c.725-1G>T	NP_000329.2:n.725-1G>T
NM_001184832.1:c.725-1G>T	NP_001171761.1:n.725-1G>T
XM_005254605.1:c.821-1G>T	XP_005254662.1:n.821-1G>T
XM_005254606.1:c.725-1G>T	XP_005254663.1:n.725-1G>T
XM_006720656.1:c.821-1G>T	XP_006720719.1:n.821-1G>T
XR_931896.1:n.1037-1G>T
XR_932203.1:n.229+768C>A
XR_932204.1:n.222+768C>A
XM_005254606.2:c.725-1G>T	XP_005254663.1:n.725-1G>T
XR_001751524.2:n.230+768C>A
XR_001751525.1:n.230+768C>A
XR_002957762.1:n.230+768C>A
XR_932204.3:n.224+768C>A
NM_000338.3:c.725-1G>T MANE Select	NP_000329.2:n.725-1G>T
NM_001184832.2:c.725-1G>T	NP_001171761.1:n.725-1G>T
NM_001384136.1:c.725-1G>T	NP_001371065.1:n.725-1G>T