Canonical Allele Identifier: CA2366499629

Gene: SLC12A5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056520T= , CM000682.2:g.46056520T=	GRCh38
NC_000020.10:g.44685159T= , CM000682.1:g.44685159T=	GRCh37
NC_000020.9:g.44118566T=	NCBI36
NG_046341.1:g.39831T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.3066T= MANE Select	ENSP00000243964.4:p.Ser1022=
ENST00000243964.6:c.3066T=	ENSP00000243964.3:p.Ser1022=
ENST00000454036.6:c.3135T=	ENSP00000387694.1:p.Ser1045=
ENST00000616201.4:c.1298-2136T=	ENSP00000484585.1:n.1298-2136T=
ENST00000616202.4:c.613-1961T=	ENSP00000478369.1:n.613-1961T=
ENST00000616933.4:c.*2384T=	ENSP00000477569.1:n.*2384T=
ENST00000626937.2:c.510-3079T=	ENSP00000485953.1:n.510-3079T=
NM_001134771.1:c.3135T=	NP_001128243.1:p.Ser1045=
NM_020708.4:c.3066T=	NP_065759.1:p.Ser1022=
XM_017027981.1:c.3135T=	XP_016883470.1:p.Ser1045=
NM_001134771.2:c.3135T=	NP_001128243.1:p.Ser1045=
NM_020708.5:c.3066T= MANE Select	NP_065759.1:p.Ser1022=