Canonical Allele Identifier: CA409207996
Gene: SLC12A5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46056502G>C , CM000682.2:g.46056502G>C GRCh38
NC_000020.10:g.44685141G>C , CM000682.1:g.44685141G>C GRCh37
NC_000020.9:g.44118548G>C NCBI36
NG_046341.1:g.39813G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000243964.7:c.3048G>C MANE Select ENSP00000243964.4:p.Glu1016Asp
ENST00000243964.6:c.3048G>C ENSP00000243964.3:p.Glu1016Asp
ENST00000454036.6:c.3117G>C ENSP00000387694.1:p.Glu1039Asp
ENST00000616201.4:c.1298-2154G>C ENSP00000484585.1:n.1298-2154G>C
ENST00000616202.4:c.613-1979G>C ENSP00000478369.1:n.613-1979G>C
ENST00000616933.4:c.*2366G>C ENSP00000477569.1:n.*2366G>C
ENST00000626937.2:c.510-3097G>C ENSP00000485953.1:n.510-3097G>C
ENST00000628413.1:n.564G>C
NM_001134771.1:c.3117G>C NP_001128243.1:p.Glu1039Asp
NM_020708.4:c.3048G>C NP_065759.1:p.Glu1016Asp
XM_017027981.1:c.3117G>C XP_016883470.1:p.Glu1039Asp
NM_001134771.2:c.3117G>C NP_001128243.1:p.Glu1039Asp
NM_020708.5:c.3048G>C MANE Select NP_065759.1:p.Glu1016Asp