Canonical Allele Identifier: CA510657408

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44685135G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056496G>T , CM000682.2:g.46056496G>T	GRCh38
NC_000020.10:g.44685135G>T , CM000682.1:g.44685135G>T	GRCh37
NC_000020.9:g.44118542G>T	NCBI36
NG_046341.1:g.39807G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.3042G>T MANE Select	ENSP00000243964.4:p.Val1014=
ENST00000243964.6:c.3042G>T	ENSP00000243964.3:p.Val1014=
ENST00000454036.6:c.3111G>T	ENSP00000387694.1:p.Val1037=
ENST00000616201.4:c.1298-2160G>T	ENSP00000484585.1:n.1298-2160G>T
ENST00000616202.4:c.613-1985G>T	ENSP00000478369.1:n.613-1985G>T
ENST00000616933.4:c.*2360G>T	ENSP00000477569.1:n.*2360G>T
ENST00000626937.2:c.510-3103G>T	ENSP00000485953.1:n.510-3103G>T
ENST00000628413.1:n.558G>T
NM_001134771.1:c.3111G>T	NP_001128243.1:p.Val1037=
NM_020708.4:c.3042G>T	NP_065759.1:p.Val1014=
XM_017027981.1:c.3111G>T	XP_016883470.1:p.Val1037=
NM_001134771.2:c.3111G>T	NP_001128243.1:p.Val1037=
NM_020708.5:c.3042G>T MANE Select	NP_065759.1:p.Val1014=