Canonical Allele Identifier: CA2366499587

Gene: SLC12A5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056413C= , CM000682.2:g.46056413C=	GRCh38
NC_000020.10:g.44685052C= , CM000682.1:g.44685052C=	GRCh37
NC_000020.9:g.44118459C=	NCBI36
NG_046341.1:g.39724C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2959C= MANE Select	ENSP00000243964.4:p.Pro987=
ENST00000243964.6:c.2959C=	ENSP00000243964.3:p.Pro987=
ENST00000454036.6:c.3028C=	ENSP00000387694.1:p.Pro1010=
ENST00000616201.4:c.1298-2243C=	ENSP00000484585.1:n.1298-2243C=
ENST00000616202.4:c.613-2068C=	ENSP00000478369.1:n.613-2068C=
ENST00000616933.4:c.*2277C=	ENSP00000477569.1:n.*2277C=
ENST00000626937.2:c.510-3186C=	ENSP00000485953.1:n.510-3186C=
ENST00000628413.1:n.475C=
NM_001134771.1:c.3028C=	NP_001128243.1:p.Pro1010=
NM_020708.4:c.2959C=	NP_065759.1:p.Pro987=
XM_017027981.1:c.3028C=	XP_016883470.1:p.Pro1010=
NM_001134771.2:c.3028C=	NP_001128243.1:p.Pro1010=
NM_020708.5:c.2959C= MANE Select	NP_065759.1:p.Pro987=