Canonical Allele Identifier: CA409207644

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44685039C>A (hg19) ; chr20:g.46056400C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056400C>A , CM000682.2:g.46056400C>A	GRCh38
NC_000020.10:g.44685039C>A , CM000682.1:g.44685039C>A	GRCh37
NC_000020.9:g.44118446C>A	NCBI36
NG_046341.1:g.39711C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2946C>A MANE Select	ENSP00000243964.4:p.Cys982Ter
ENST00000243964.6:c.2946C>A	ENSP00000243964.3:p.Cys982Ter
ENST00000454036.6:c.3015C>A	ENSP00000387694.1:p.Cys1005Ter
ENST00000616201.4:c.1298-2256C>A	ENSP00000484585.1:n.1298-2256C>A
ENST00000616202.4:c.613-2081C>A	ENSP00000478369.1:n.613-2081C>A
ENST00000616933.4:c.*2264C>A	ENSP00000477569.1:n.*2264C>A
ENST00000626937.2:c.510-3199C>A	ENSP00000485953.1:n.510-3199C>A
ENST00000628413.1:n.462C>A
NM_001134771.1:c.3015C>A	NP_001128243.1:p.Cys1005Ter
NM_020708.4:c.2946C>A	NP_065759.1:p.Cys982Ter
XM_017027981.1:c.3015C>A	XP_016883470.1:p.Cys1005Ter
NM_001134771.2:c.3015C>A	NP_001128243.1:p.Cys1005Ter
NM_020708.5:c.2946C>A MANE Select	NP_065759.1:p.Cys982Ter