Canonical Allele Identifier: CA657646684

Gene: SLC12A5

Linked Data

• COSMIC: COSN17886821

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46055800C>T , CM000682.2:g.46055800C>T	GRCh38
NC_000020.10:g.44684439C>T , CM000682.1:g.44684439C>T	GRCh37
NC_000020.9:g.44117846C>T	NCBI36
NG_046341.1:g.39111C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000243964.7:c.2788-350C>T MANE Select	ENSP00000243964.4:n.2788-350C>T
ENST00000243964.6:c.2788-350C>T	ENSP00000243964.3:n.2788-350C>T
ENST00000454036.6:c.2857-350C>T	ENSP00000387694.1:n.2857-350C>T
ENST00000616201.4:c.1298-2856C>T	ENSP00000484585.1:n.1298-2856C>T
ENST00000616202.4:c.613-2681C>T	ENSP00000478369.1:n.613-2681C>T
ENST00000616933.4:c.*2106-350C>T	ENSP00000477569.1:n.*2106-350C>T
ENST00000626937.2:c.510-3799C>T	ENSP00000485953.1:n.510-3799C>T
NM_001134771.1:c.2857-350C>T	NP_001128243.1:n.2857-350C>T
NM_020708.4:c.2788-350C>T	NP_065759.1:n.2788-350C>T
XM_017027981.1:c.2857-350C>T	XP_016883470.1:n.2857-350C>T
NM_001134771.2:c.2857-350C>T	NP_001128243.1:n.2857-350C>T
NM_020708.5:c.2788-350C>T MANE Select	NP_065759.1:n.2788-350C>T