Canonical Allele Identifier: CA2674167218

Gene: MCCC2

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71646120G>T , CM000667.2:g.71646120G>T	GRCh38
NC_000005.9:g.70941947G>T , CM000667.1:g.70941947G>T	GRCh37
NC_000005.8:g.70977703G>T	NCBI36
NG_008882.1:g.63833G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.2758-91G>T
ENST00000505787.8:n.2981-91G>T
ENST00000509539.3:c.476-91G>T	ENSP00000425474.3:n.476-91G>T
ENST00000681968.1:c.643-91G>T	ENSP00000508143.1:n.643-91G>T
ENST00000681991.1:n.1234-91G>T
ENST00000682045.1:c.1006-91G>T	ENSP00000507329.1:n.1006-91G>T
ENST00000682214.1:c.757-91G>T	ENSP00000507336.1:n.757-91G>T
ENST00000682231.1:n.168-91G>T
ENST00000682438.1:n.3058G>T
ENST00000682499.1:n.1971-91G>T
ENST00000682541.1:c.*48-91G>T	ENSP00000507673.1:n.*48-91G>T
ENST00000682640.1:n.854-91G>T
ENST00000682667.1:n.1315-91G>T
ENST00000682687.1:c.*102-91G>T	ENSP00000507945.1:n.*102-91G>T
ENST00000682727.1:c.1141-91G>T	ENSP00000507393.1:n.1141-91G>T
ENST00000682876.1:c.1279-91G>T	ENSP00000508389.1:n.1279-91G>T
ENST00000683098.1:c.804-91G>T	ENSP00000507670.1:n.804-91G>T
ENST00000683258.1:c.*871-91G>T	ENSP00000507448.1:n.*871-91G>T
ENST00000683339.1:c.934-91G>T	ENSP00000507758.1:n.934-91G>T
ENST00000683403.1:c.1060-91G>T	ENSP00000507896.1:n.1060-91G>T
ENST00000683429.1:c.757-91G>T	ENSP00000507697.1:n.757-91G>T
ENST00000683789.1:c.1036-91G>T	ENSP00000507012.1:n.1036-91G>T
ENST00000683847.1:n.1320-91G>T
ENST00000683882.1:c.*91-91G>T	ENSP00000506735.1:n.*91-91G>T
ENST00000684024.1:c.*821-91G>T	ENSP00000507175.1:n.*821-91G>T
ENST00000684132.1:c.78-91G>T
ENST00000684254.1:c.*876-91G>T	ENSP00000508001.1:n.*876-91G>T
ENST00000684310.1:c.316-91G>T	ENSP00000507550.1:n.316-91G>T
ENST00000684474.1:n.786-91G>T
ENST00000684530.1:c.335-2977G>T	ENSP00000507439.1:n.335-2977G>T
ENST00000684686.1:n.769-91G>T
ENST00000340941.11:c.1150-91G>T MANE Select	ENSP00000343657.6:n.1150-91G>T
ENST00000340941.10:c.1150-91G>T	ENSP00000343657.6:n.1150-91G>T
ENST00000509539.2:c.466-91G>T	ENSP00000425474.2:n.466-91G>T
ENST00000512218.6:c.*102-91G>T	ENSP00000423202.2:n.*102-91G>T
NM_022132.4:c.1150-91G>T	NP_071415.1:n.1150-91G>T
XM_005248567.1:c.1036-91G>T	XP_005248624.1:n.1036-91G>T
NM_001363147.1:c.1036-91G>T	NP_001350076.1:n.1036-91G>T
XR_001742172.1:n.1238-91G>T
NM_022132.5:c.1150-91G>T MANE Select	NP_071415.1:n.1150-91G>T