Canonical Allele Identifier: CA658657454
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71649247_71649248delinsTG , CM000667.2:g.71649247_71649248delinsTG GRCh38
NC_000005.9:g.70945074_70945075delinsTG , CM000667.1:g.70945074_70945075delinsTG GRCh37
NC_000005.8:g.70980830_70980831delinsTG NCBI36
NG_008882.1:g.66960_66961delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.2975_2976delinsTG
ENST00000505787.8:n.3198_3199delinsTG
ENST00000509539.3:c.693_694delinsTG ENSP00000425474.3:n.693_694delinsTG
ENST00000681968.1:c.860_861delinsTG ENSP00000508143.1:p.Ala287Val
ENST00000681991.1:n.1451_1452delinsTG
ENST00000682045.1:c.1223_1224delinsTG ENSP00000507329.1:p.Ala408Val
ENST00000682214.1:c.974_975delinsTG ENSP00000507336.1:p.Ala325Val
ENST00000682231.1:n.385_386delinsTG
ENST00000682438.1:n.3366_3367delinsTG
ENST00000682499.1:n.2188_2189delinsTG
ENST00000682541.1:c.*265_*266delinsTG ENSP00000507673.1:n.*265_*266delinsTG
ENST00000682640.1:n.1071_1072delinsTG
ENST00000682667.1:n.1559_1560delinsTG
ENST00000682687.1:c.*319_*320delinsTG ENSP00000507945.1:n.*319_*320delinsTG
ENST00000682727.1:c.1358_1359delinsTG ENSP00000507393.1:p.Ala453Val
ENST00000682876.1:c.1496_1497delinsTG ENSP00000508389.1:p.Ala499Val
ENST00000683098.1:c.*55_*56delinsTG ENSP00000507670.1:n.*55_*56delinsTG
ENST00000683258.1:c.*1088_*1089delinsTG ENSP00000507448.1:n.*1088_*1089delinsTG
ENST00000683339.1:c.1151_1152delinsTG ENSP00000507758.1:p.Ala384Val
ENST00000683403.1:c.1277_1278delinsTG ENSP00000507896.1:p.Ala426Val
ENST00000683429.1:c.974_975delinsTG ENSP00000507697.1:p.Ala325Val
ENST00000683789.1:c.1253_1254delinsTG ENSP00000507012.1:p.Ala418Val
ENST00000683847.1:n.1537_1538delinsTG
ENST00000683882.1:c.*308_*309delinsTG ENSP00000506735.1:n.*308_*309delinsTG
ENST00000684024.1:c.*1038_*1039delinsTG ENSP00000507175.1:n.*1038_*1039delinsTG
ENST00000684132.1:c.295_296delinsTG
ENST00000684254.1:c.*1093_*1094delinsTG ENSP00000508001.1:n.*1093_*1094delinsTG
ENST00000684310.1:c.533_534delinsTG ENSP00000507550.1:p.Ala178Val
ENST00000684316.1:n.205_206delinsTG
ENST00000684474.1:n.1003_1004delinsTG
ENST00000684530.1:c.485_486delinsTG ENSP00000507439.1:p.Ala162Val
ENST00000684686.1:n.986_987delinsTG
ENST00000340941.11:c.1367_1368delinsTG MANE Select ENSP00000343657.6:p.Ala456Val
ENST00000340941.10:c.1367_1368delinsTG ENSP00000343657.6:p.Ala456Val
ENST00000509539.2:c.683_684delinsTG ENSP00000425474.2:p.Ala228Val
ENST00000512218.6:c.*319_*320delinsTG ENSP00000423202.2:n.*319_*320delinsTG
NM_022132.4:c.1367_1368delinsTG NP_071415.1:p.Ala456Val
XM_005248567.1:c.1253_1254delinsTG XP_005248624.1:p.Ala418Val
NM_001363147.1:c.1253_1254delinsTG NP_001350076.1:p.Ala418Val
XR_001742172.1:n.1455_1456delinsTG
NM_022132.5:c.1367_1368delinsTG MANE Select NP_071415.1:p.Ala456Val