Canonical Allele Identifier: CA409207516

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44684901C>A (hg19) ; chr20:g.46056262C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056262C>A , CM000682.2:g.46056262C>A	GRCh38
NC_000020.10:g.44684901C>A , CM000682.1:g.44684901C>A	GRCh37
NC_000020.9:g.44118308C>A	NCBI36
NG_046341.1:g.39573C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2900C>A MANE Select	ENSP00000243964.4:p.Pro967Gln
ENST00000243964.6:c.2900C>A	ENSP00000243964.3:p.Pro967Gln
ENST00000454036.6:c.2969C>A	ENSP00000387694.1:p.Pro990Gln
ENST00000616201.4:c.1298-2394C>A	ENSP00000484585.1:n.1298-2394C>A
ENST00000616202.4:c.613-2219C>A	ENSP00000478369.1:n.613-2219C>A
ENST00000616933.4:c.*2218C>A	ENSP00000477569.1:n.*2218C>A
ENST00000626937.2:c.510-3337C>A	ENSP00000485953.1:n.510-3337C>A
ENST00000628413.1:n.416C>A
NM_001134771.1:c.2969C>A	NP_001128243.1:p.Pro990Gln
NM_020708.4:c.2900C>A	NP_065759.1:p.Pro967Gln
XM_017027981.1:c.2969C>A	XP_016883470.1:p.Pro990Gln
NM_001134771.2:c.2969C>A	NP_001128243.1:p.Pro990Gln
NM_020708.5:c.2900C>A MANE Select	NP_065759.1:p.Pro967Gln