Canonical Allele Identifier: CA409207586

Gene: SLC12A5

Linked Data

• MyVariant Identifiers: chr20:g.44685019G>T (hg19) ; chr20:g.46056380G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46056380G>T , CM000682.2:g.46056380G>T	GRCh38
NC_000020.10:g.44685019G>T , CM000682.1:g.44685019G>T	GRCh37
NC_000020.9:g.44118426G>T	NCBI36
NG_046341.1:g.39691G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2926G>T MANE Select	ENSP00000243964.4:p.Asp976Tyr
ENST00000243964.6:c.2926G>T	ENSP00000243964.3:p.Asp976Tyr
ENST00000454036.6:c.2995G>T	ENSP00000387694.1:p.Asp999Tyr
ENST00000616201.4:c.1298-2276G>T	ENSP00000484585.1:n.1298-2276G>T
ENST00000616202.4:c.613-2101G>T	ENSP00000478369.1:n.613-2101G>T
ENST00000616933.4:c.*2244G>T	ENSP00000477569.1:n.*2244G>T
ENST00000626937.2:c.510-3219G>T	ENSP00000485953.1:n.510-3219G>T
ENST00000628413.1:n.442G>T
NM_001134771.1:c.2995G>T	NP_001128243.1:p.Asp999Tyr
NM_020708.4:c.2926G>T	NP_065759.1:p.Asp976Tyr
XM_017027981.1:c.2995G>T	XP_016883470.1:p.Asp999Tyr
NM_001134771.2:c.2995G>T	NP_001128243.1:p.Asp999Tyr
NM_020708.5:c.2926G>T MANE Select	NP_065759.1:p.Asp976Tyr