Canonical Allele Identifier: CA2366499502
Gene: SLC12A5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46056213C= , CM000682.2:g.46056213C= GRCh38
NC_000020.10:g.44684852C= , CM000682.1:g.44684852C= GRCh37
NC_000020.9:g.44118259C= NCBI36
NG_046341.1:g.39524C=

Transcript Alleles

HGVS Amino-acid change
ENST00000243964.7:c.2851C= MANE Select ENSP00000243964.4:p.Leu951=
ENST00000243964.6:c.2851C= ENSP00000243964.3:p.Leu951=
ENST00000454036.6:c.2920C= ENSP00000387694.1:p.Leu974=
ENST00000616201.4:c.1298-2443C= ENSP00000484585.1:n.1298-2443C=
ENST00000616202.4:c.613-2268C= ENSP00000478369.1:n.613-2268C=
ENST00000616933.4:c.*2169C= ENSP00000477569.1:n.*2169C=
ENST00000626937.2:c.510-3386C= ENSP00000485953.1:n.510-3386C=
ENST00000628413.1:n.367C=
NM_001134771.1:c.2920C= NP_001128243.1:p.Leu974=
NM_020708.4:c.2851C= NP_065759.1:p.Leu951=
XM_017027981.1:c.2920C= XP_016883470.1:p.Leu974=
NM_001134771.2:c.2920C= NP_001128243.1:p.Leu974=
NM_020708.5:c.2851C= MANE Select NP_065759.1:p.Leu951=