Canonical Allele Identifier: CA244361911

Gene: CIT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119720715A>T , CM000674.2:g.119720715A>T	GRCh38
NC_000012.11:g.120158520A>T , CM000674.1:g.120158520A>T	GRCh37
NC_000012.10:g.118642903A>T	NCBI36
NG_029792.1:g.161576T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392521.7:c.3733-130T>A MANE Select	ENSP00000376306.2:n.3733-130T>A
ENST00000543324.2:n.290-130T>A
ENST00000545913.6:n.2723-130T>A
ENST00000676693.1:n.1195-130T>A
ENST00000676833.1:n.2895-130T>A
ENST00000676849.1:c.2395-130T>A	ENSP00000503214.1:n.2395-130T>A
ENST00000677438.1:c.*2884-130T>A	ENSP00000504095.1:n.*2884-130T>A
ENST00000677738.1:n.930-130T>A
ENST00000677812.1:c.*3010-130T>A	ENSP00000504400.1:n.*3010-130T>A
ENST00000677849.1:c.*2884-130T>A	ENSP00000503820.1:n.*2884-130T>A
ENST00000677993.1:c.2395-130T>A	ENSP00000503765.1:n.2395-130T>A
ENST00000678087.1:c.2269-130T>A	ENSP00000503863.1:n.2269-130T>A
ENST00000678236.1:n.2020-130T>A
ENST00000678494.1:c.1227-33681T>A	ENSP00000503854.1:n.1227-33681T>A
ENST00000678652.1:c.2395-130T>A	ENSP00000504849.1:n.2395-130T>A
ENST00000678677.1:c.2395-130T>A	ENSP00000503253.1:n.2395-130T>A
ENST00000679120.1:c.*1785-130T>A	ENSP00000502891.1:n.*1785-130T>A
ENST00000679249.1:c.2395-130T>A	ENSP00000503976.1:n.2395-130T>A
ENST00000679285.1:n.1229-130T>A
ENST00000261833.11:c.3607-130T>A	ENSP00000261833.7:n.3607-130T>A
ENST00000392520.2:c.2490-130T>A
ENST00000392521.6:c.3733-130T>A	ENSP00000376306.2:n.3733-130T>A
ENST00000536325.1:c.268-130T>A	ENSP00000443199.1:n.268-130T>A
ENST00000537607.5:n.2505-130T>A
ENST00000545913.5:n.3649-130T>A
ENST00000612548.4:c.1442-32651T>A	ENSP00000482318.1:n.1442-32651T>A
NM_001206999.1:c.3733-130T>A	NP_001193928.1:n.3733-130T>A
NM_007174.2:c.3607-130T>A	NP_009105.1:n.3607-130T>A
XM_006719206.2:c.3733-130T>A	XP_006719269.1:n.3733-130T>A
XM_011537783.1:c.3733-130T>A	XP_011536085.1:n.3733-130T>A
XM_011537784.1:c.3733-130T>A	XP_011536086.1:n.3733-130T>A
XM_011537785.1:c.3733-130T>A	XP_011536087.1:n.3733-130T>A
XM_011537786.1:c.3607-130T>A	XP_011536088.1:n.3607-130T>A
XM_011537787.1:c.3607-130T>A	XP_011536089.1:n.3607-130T>A
XM_011537788.1:c.3607-130T>A	XP_011536090.1:n.3607-130T>A
XM_011537789.1:c.2395-130T>A	XP_011536091.1:n.2395-130T>A
XM_011537790.1:c.2395-130T>A	XP_011536092.1:n.2395-130T>A
XM_011537791.1:c.2335-130T>A	XP_011536093.1:n.2335-130T>A
XM_011537792.1:c.2209-130T>A	XP_011536094.1:n.2209-130T>A
XM_011537790.2:c.2395-130T>A	XP_011536092.1:n.2395-130T>A
XM_011537791.2:c.2335-130T>A	XP_011536093.1:n.2335-130T>A
XM_011537792.2:c.2209-130T>A	XP_011536094.1:n.2209-130T>A
XM_017018735.1:c.3733-130T>A	XP_016874224.1:n.3733-130T>A
XM_017018736.1:c.3733-130T>A	XP_016874225.1:n.3733-130T>A
XM_017018737.1:c.3733-130T>A	XP_016874226.1:n.3733-130T>A
XM_017018738.1:c.2209-130T>A	XP_016874227.1:n.2209-130T>A
XM_017018739.1:c.2209-130T>A	XP_016874228.1:n.2209-130T>A
NM_001206999.2:c.3733-130T>A MANE Select	NP_001193928.1:n.3733-130T>A
NM_007174.3:c.3607-130T>A	NP_009105.1:n.3607-130T>A