Canonical Allele Identifier: CA6821051

Gene: CIT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119710521G>A , CM000674.2:g.119710521G>A	GRCh38
NC_000012.11:g.120148326G>A , CM000674.1:g.120148326G>A	GRCh37
NC_000012.10:g.118632709G>A	NCBI36
NG_029792.1:g.171770C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392521.7:c.4935+19C>T MANE Select	ENSP00000376306.2:n.4935+19C>T
ENST00000543324.2:n.1492+19C>T
ENST00000545913.6:n.7098+19C>T
ENST00000676693.1:n.2397+19C>T
ENST00000676833.1:n.4295+19C>T
ENST00000676849.1:c.3552+19C>T	ENSP00000503214.1:n.3552+19C>T
ENST00000677438.1:c.*4041+19C>T	ENSP00000504095.1:n.*4041+19C>T
ENST00000677738.1:n.2132+19C>T
ENST00000677742.1:n.245+19C>T
ENST00000677812.1:c.*4155+19C>T	ENSP00000504400.1:n.*4155+19C>T
ENST00000677849.1:c.*4041+19C>T	ENSP00000503820.1:n.*4041+19C>T
ENST00000677993.1:c.3540+19C>T	ENSP00000503765.1:n.3540+19C>T
ENST00000678087.1:c.3426+19C>T	ENSP00000503863.1:n.3426+19C>T
ENST00000678236.1:n.6395+19C>T
ENST00000678494.1:c.1227-23487C>T	ENSP00000503854.1:n.1227-23487C>T
ENST00000678652.1:c.3552+19C>T	ENSP00000504849.1:n.3552+19C>T
ENST00000678677.1:c.3339+19C>T	ENSP00000503253.1:n.3339+19C>T
ENST00000679120.1:c.*2942+19C>T	ENSP00000502891.1:n.*2942+19C>T
ENST00000679249.1:c.3552+19C>T	ENSP00000503976.1:n.3552+19C>T
ENST00000679285.1:n.2431+19C>T
ENST00000261833.11:c.4809+19C>T	ENSP00000261833.7:n.4809+19C>T
ENST00000392520.2:c.3647+19C>T
ENST00000392521.6:c.4935+19C>T	ENSP00000376306.2:n.4935+19C>T
ENST00000537607.5:n.3662+19C>T
ENST00000538073.5:n.193+19C>T
ENST00000543324.1:n.127+19C>T
ENST00000544800.1:n.472+19C>T
ENST00000545913.5:n.4806+19C>T
ENST00000612548.4:c.1442-22457C>T	ENSP00000482318.1:n.1442-22457C>T
NM_001206999.1:c.4935+19C>T	NP_001193928.1:n.4935+19C>T
NM_007174.2:c.4809+19C>T	NP_009105.1:n.4809+19C>T
XM_006719206.2:c.4890+19C>T	XP_006719269.1:n.4890+19C>T
XM_011537783.1:c.4980+19C>T	XP_011536085.1:n.4980+19C>T
XM_011537784.1:c.4980+19C>T	XP_011536086.1:n.4980+19C>T
XM_011537785.1:c.4935+19C>T	XP_011536087.1:n.4935+19C>T
XM_011537786.1:c.4854+19C>T	XP_011536088.1:n.4854+19C>T
XM_011537787.1:c.4764+19C>T	XP_011536089.1:n.4764+19C>T
XM_011537788.1:c.4764+19C>T	XP_011536090.1:n.4764+19C>T
XM_011537789.1:c.3642+19C>T	XP_011536091.1:n.3642+19C>T
XM_011537790.1:c.3642+19C>T	XP_011536092.1:n.3642+19C>T
XM_011537791.1:c.3582+19C>T	XP_011536093.1:n.3582+19C>T
XM_011537792.1:c.3366+19C>T	XP_011536094.1:n.3366+19C>T
XM_011537790.2:c.3642+19C>T	XP_011536092.1:n.3642+19C>T
XM_011537791.2:c.3582+19C>T	XP_011536093.1:n.3582+19C>T
XM_011537792.2:c.3366+19C>T	XP_011536094.1:n.3366+19C>T
XM_017018735.1:c.4935+19C>T	XP_016874224.1:n.4935+19C>T
XM_017018736.1:c.4935+19C>T	XP_016874225.1:n.4935+19C>T
XM_017018737.1:c.4890+19C>T	XP_016874226.1:n.4890+19C>T
XM_017018738.1:c.3456+19C>T	XP_016874227.1:n.3456+19C>T
XM_017018739.1:c.3366+19C>T	XP_016874228.1:n.3366+19C>T
NM_001206999.2:c.4935+19C>T MANE Select	NP_001193928.1:n.4935+19C>T
NM_007174.3:c.4809+19C>T	NP_009105.1:n.4809+19C>T