Canonical Allele Identifier: CA1554397144
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71646135_71646138delinsTGTG , CM000667.2:g.71646135_71646138delinsTGTG GRCh38
NC_000005.9:g.70941962_70941965delinsTGTG , CM000667.1:g.70941962_70941965delinsTGTG GRCh37
NC_000005.8:g.70977718_70977721delinsTGTG NCBI36
NG_008882.1:g.63848_63851delinsTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.2758-76_2758-73delinsTGTG
ENST00000505787.8:n.2981-76_2981-73delinsTGTG
ENST00000509539.3:c.476-76_476-73delinsTGTG ENSP00000425474.3:n.476-76_476-73delinsTGTG
ENST00000681968.1:c.643-76_643-73delinsTGTG ENSP00000508143.1:n.643-76_643-73delinsTGTG
ENST00000681991.1:n.1234-76_1234-73delinsTGTG
ENST00000682045.1:c.1006-76_1006-73delinsTGTG ENSP00000507329.1:n.1006-76_1006-73delinsTGTG
ENST00000682214.1:c.757-76_757-73delinsTGTG ENSP00000507336.1:n.757-76_757-73delinsTGTG
ENST00000682231.1:n.168-76_168-73delinsTGTG
ENST00000682438.1:n.3073_3076delinsTGTG
ENST00000682499.1:n.1971-76_1971-73delinsTGTG
ENST00000682541.1:c.*48-76_*48-73delinsTGTG ENSP00000507673.1:n.*48-76_*48-73delinsTGTG
ENST00000682640.1:n.854-76_854-73delinsTGTG
ENST00000682667.1:n.1315-76_1315-73delinsTGTG
ENST00000682687.1:c.*102-76_*102-73delinsTGTG ENSP00000507945.1:n.*102-76_*102-73delinsTGTG
ENST00000682727.1:c.1141-76_1141-73delinsTGTG ENSP00000507393.1:n.1141-76_1141-73delinsTGTG
ENST00000682876.1:c.1279-76_1279-73delinsTGTG ENSP00000508389.1:n.1279-76_1279-73delinsTGTG
ENST00000683098.1:c.804-76_804-73delinsTGTG ENSP00000507670.1:n.804-76_804-73delinsTGTG
ENST00000683258.1:c.*871-76_*871-73delinsTGTG ENSP00000507448.1:n.*871-76_*871-73delinsTGTG
ENST00000683339.1:c.934-76_934-73delinsTGTG ENSP00000507758.1:n.934-76_934-73delinsTGTG
ENST00000683403.1:c.1060-76_1060-73delinsTGTG ENSP00000507896.1:n.1060-76_1060-73delinsTGTG
ENST00000683429.1:c.757-76_757-73delinsTGTG ENSP00000507697.1:n.757-76_757-73delinsTGTG
ENST00000683789.1:c.1036-76_1036-73delinsTGTG ENSP00000507012.1:n.1036-76_1036-73delinsTGTG
ENST00000683847.1:n.1320-76_1320-73delinsTGTG
ENST00000683882.1:c.*91-76_*91-73delinsTGTG ENSP00000506735.1:n.*91-76_*91-73delinsTGTG
ENST00000684024.1:c.*821-76_*821-73delinsTGTG ENSP00000507175.1:n.*821-76_*821-73delinsTGTG
ENST00000684132.1:c.78-76_78-73delinsTGTG
ENST00000684254.1:c.*876-76_*876-73delinsTGTG ENSP00000508001.1:n.*876-76_*876-73delinsTGTG
ENST00000684310.1:c.316-76_316-73delinsTGTG ENSP00000507550.1:n.316-76_316-73delinsTGTG
ENST00000684474.1:n.786-76_786-73delinsTGTG
ENST00000684530.1:c.335-2962_335-2959delinsTGTG ENSP00000507439.1:n.335-2962_335-2959delinsTGTG
ENST00000684686.1:n.769-76_769-73delinsTGTG
ENST00000340941.11:c.1150-76_1150-73delinsTGTG MANE Select ENSP00000343657.6:n.1150-76_1150-73delinsTGTG
ENST00000340941.10:c.1150-76_1150-73delinsTGTG ENSP00000343657.6:n.1150-76_1150-73delinsTGTG
ENST00000509539.2:c.466-76_466-73delinsTGTG ENSP00000425474.2:n.466-76_466-73delinsTGTG
ENST00000512218.6:c.*102-76_*102-73delinsTGTG ENSP00000423202.2:n.*102-76_*102-73delinsTGTG
NM_022132.4:c.1150-76_1150-73delinsTGTG NP_071415.1:n.1150-76_1150-73delinsTGTG
XM_005248567.1:c.1036-76_1036-73delinsTGTG XP_005248624.1:n.1036-76_1036-73delinsTGTG
NM_001363147.1:c.1036-76_1036-73delinsTGTG NP_001350076.1:n.1036-76_1036-73delinsTGTG
XR_001742172.1:n.1238-76_1238-73delinsTGTG
NM_022132.5:c.1150-76_1150-73delinsTGTG MANE Select NP_071415.1:n.1150-76_1150-73delinsTGTG