Canonical Allele Identifier: CA409207451

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44684872A>C (hg19) ; chr20:g.46056233A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056233A>C , CM000682.2:g.46056233A>C	GRCh38
NC_000020.10:g.44684872A>C , CM000682.1:g.44684872A>C	GRCh37
NC_000020.9:g.44118279A>C	NCBI36
NG_046341.1:g.39544A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2871A>C MANE Select	ENSP00000243964.4:p.Glu957Asp
ENST00000243964.6:c.2871A>C	ENSP00000243964.3:p.Glu957Asp
ENST00000454036.6:c.2940A>C	ENSP00000387694.1:p.Glu980Asp
ENST00000616201.4:c.1298-2423A>C	ENSP00000484585.1:n.1298-2423A>C
ENST00000616202.4:c.613-2248A>C	ENSP00000478369.1:n.613-2248A>C
ENST00000616933.4:c.*2189A>C	ENSP00000477569.1:n.*2189A>C
ENST00000626937.2:c.510-3366A>C	ENSP00000485953.1:n.510-3366A>C
ENST00000628413.1:n.387A>C
NM_001134771.1:c.2940A>C	NP_001128243.1:p.Glu980Asp
NM_020708.4:c.2871A>C	NP_065759.1:p.Glu957Asp
XM_017027981.1:c.2940A>C	XP_016883470.1:p.Glu980Asp
NM_001134771.2:c.2940A>C	NP_001128243.1:p.Glu980Asp
NM_020708.5:c.2871A>C MANE Select	NP_065759.1:p.Glu957Asp