Canonical Allele Identifier: CA2067156529

Gene: CIT

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119833296T= , CM000674.2:g.119833296T=	GRCh38
NC_000012.11:g.120271100T= , CM000674.1:g.120271100T=	GRCh37
NC_000012.10:g.118755483T=	NCBI36
NG_029792.1:g.48996A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392521.7:c.660-432A= MANE Select	ENSP00000376306.2:n.660-432A=
ENST00000261833.11:c.660-432A=	ENSP00000261833.7:n.660-432A=
ENST00000392521.6:c.660-432A=	ENSP00000376306.2:n.660-432A=
ENST00000536325.1:c.267+16878A=	ENSP00000443199.1:n.267+16878A=
ENST00000612548.4:c.660-432A=	ENSP00000482318.1:n.660-432A=
NM_001206999.1:c.660-432A=	NP_001193928.1:n.660-432A=
NM_007174.2:c.660-432A=	NP_009105.1:n.660-432A=
XM_006719206.2:c.660-432A=	XP_006719269.1:n.660-432A=
XM_011537783.1:c.660-432A=	XP_011536085.1:n.660-432A=
XM_011537784.1:c.660-432A=	XP_011536086.1:n.660-432A=
XM_011537785.1:c.660-432A=	XP_011536087.1:n.660-432A=
XM_011537786.1:c.660-432A=	XP_011536088.1:n.660-432A=
XM_011537787.1:c.660-432A=	XP_011536089.1:n.660-432A=
XM_011537788.1:c.660-432A=	XP_011536090.1:n.660-432A=
XM_017018735.1:c.660-432A=	XP_016874224.1:n.660-432A=
XM_017018736.1:c.660-432A=	XP_016874225.1:n.660-432A=
XM_017018737.1:c.660-432A=	XP_016874226.1:n.660-432A=
NM_001206999.2:c.660-432A= MANE Select	NP_001193928.1:n.660-432A=
NM_007174.3:c.660-432A=	NP_009105.1:n.660-432A=