Canonical Allele Identifier: CA2573157122

Gene: SLC12A5

Linked Data

• ClinVar Variation Id: 1662375
• ClinVar RCV Id: RCV002185689
• dbSNP Id: rs2145507462

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056142C>T , CM000682.2:g.46056142C>T	GRCh38
NC_000020.10:g.44684781C>T , CM000682.1:g.44684781C>T	GRCh37
NC_000020.9:g.44118188C>T	NCBI36
NG_046341.1:g.39453C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2788-8C>T MANE Select	ENSP00000243964.4:n.2788-8C>T
ENST00000243964.6:c.2788-8C>T	ENSP00000243964.3:n.2788-8C>T
ENST00000454036.6:c.2857-8C>T	ENSP00000387694.1:n.2857-8C>T
ENST00000616201.4:c.1298-2514C>T	ENSP00000484585.1:n.1298-2514C>T
ENST00000616202.4:c.613-2339C>T	ENSP00000478369.1:n.613-2339C>T
ENST00000616933.4:c.*2106-8C>T	ENSP00000477569.1:n.*2106-8C>T
ENST00000626937.2:c.510-3457C>T	ENSP00000485953.1:n.510-3457C>T
ENST00000628413.1:n.296C>T
NM_001134771.1:c.2857-8C>T	NP_001128243.1:n.2857-8C>T
NM_020708.4:c.2788-8C>T	NP_065759.1:n.2788-8C>T
XM_017027981.1:c.2857-8C>T	XP_016883470.1:n.2857-8C>T
NM_001134771.2:c.2857-8C>T	NP_001128243.1:n.2857-8C>T
NM_020708.5:c.2788-8C>T MANE Select	NP_065759.1:n.2788-8C>T