Canonical Allele Identifier: CA409208171

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44685175G>C (hg19) ; chr20:g.46056536G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056536G>C , CM000682.2:g.46056536G>C	GRCh38
NC_000020.10:g.44685175G>C , CM000682.1:g.44685175G>C	GRCh37
NC_000020.9:g.44118582G>C	NCBI36
NG_046341.1:g.39847G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.3082G>C MANE Select	ENSP00000243964.4:p.Gly1028Arg
ENST00000243964.6:c.3082G>C	ENSP00000243964.3:p.Gly1028Arg
ENST00000454036.6:c.3151G>C	ENSP00000387694.1:p.Gly1051Arg
ENST00000616201.4:c.1298-2120G>C	ENSP00000484585.1:n.1298-2120G>C
ENST00000616202.4:c.613-1945G>C	ENSP00000478369.1:n.613-1945G>C
ENST00000616933.4:c.*2400G>C	ENSP00000477569.1:n.*2400G>C
ENST00000626937.2:c.510-3063G>C	ENSP00000485953.1:n.510-3063G>C
NM_001134771.1:c.3151G>C	NP_001128243.1:p.Gly1051Arg
NM_020708.4:c.3082G>C	NP_065759.1:p.Gly1028Arg
XM_017027981.1:c.3151G>C	XP_016883470.1:p.Gly1051Arg
NM_001134771.2:c.3151G>C	NP_001128243.1:p.Gly1051Arg
NM_020708.5:c.3082G>C MANE Select	NP_065759.1:p.Gly1028Arg