Canonical Allele Identifier: CA2175394371

Gene: SLC12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48229326A= , CM000677.2:g.48229326A=	GRCh38
NC_000015.9:g.48521523A= , CM000677.1:g.48521523A=	GRCh37
NC_000015.8:g.46308815A=	NCBI36
NG_021301.1:g.28026A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000686073.1:c.862A=	ENSP00000508901.1:p.Lys288=
ENST00000380993.8:c.862A= MANE Select	ENSP00000370381.3:p.Lys288=
ENST00000646012.1:c.1000A=	ENSP00000495813.1:p.Lys334=
ENST00000647232.1:c.862A=	ENSP00000493875.1:p.Lys288=
ENST00000647546.1:c.862A=	ENSP00000495332.1:p.Lys288=
ENST00000330289.10:c.862A=	ENSP00000331550.6:p.Lys288=
ENST00000380993.7:c.862A=	ENSP00000370381.3:p.Lys288=
ENST00000396577.7:c.862A=	ENSP00000379822.3:p.Lys288=
ENST00000558252.5:n.4985A=
ENST00000558405.5:c.862A=	ENSP00000453409.1:p.Lys288=
ENST00000559641.5:c.301A=	ENSP00000453230.1:p.Lys101=
ENST00000559723.2:n.235A=
ENST00000560692.5:n.5001A=
ENST00000561127.5:c.301A=	ENSP00000453602.2:p.Lys101=
NM_000338.2:c.862A=	NP_000329.2:p.Lys288=
NM_001184832.1:c.862A=	NP_001171761.1:p.Lys288=
XM_005254605.1:c.958A=	XP_005254662.1:p.Lys320=
XM_005254606.1:c.862A=	XP_005254663.1:p.Lys288=
XM_006720656.1:c.958A=	XP_006720719.1:p.Lys320=
XR_931896.1:n.1174A=
XR_932203.1:n.229+630T=
XR_932204.1:n.222+630T=
XM_005254606.2:c.862A=	XP_005254663.1:p.Lys288=
XR_001751524.2:n.230+630T=
XR_001751525.1:n.230+630T=
XR_002957762.1:n.230+630T=
XR_932204.3:n.224+630T=
NM_000338.3:c.862A= MANE Select	NP_000329.2:p.Lys288=
NM_001184832.2:c.862A=	NP_001171761.1:p.Lys288=
NM_001384136.1:c.862A=	NP_001371065.1:p.Lys288=