Canonical Allele Identifier: CA359986109

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930778G>T (hg19) ; chr5:g.71634951G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634951G>T , CM000667.2:g.71634951G>T	GRCh38
NC_000005.9:g.70930778G>T , CM000667.1:g.70930778G>T	GRCh37
NC_000005.8:g.70966534G>T	NCBI36
NG_008882.1:g.52664G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.768G>T
ENST00000505787.8:n.2652G>T
ENST00000509358.7:c.812G>T	ENSP00000420994.3:p.Gly271Val
ENST00000509539.3:c.74G>T	ENSP00000425474.3:p.Gly25Val
ENST00000510895.7:n.935G>T
ENST00000629193.3:c.698G>T	ENSP00000486535.2:p.Gly233Val
ENST00000681968.1:c.305G>T	ENSP00000508143.1:p.Gly102Val
ENST00000682045.1:c.668G>T	ENSP00000507329.1:p.Gly223Val
ENST00000682214.1:c.419G>T	ENSP00000507336.1:p.Gly140Val
ENST00000682499.1:n.1633G>T
ENST00000682541.1:c.812G>T	ENSP00000507673.1:p.Gly271Val
ENST00000682687.1:c.812G>T	ENSP00000507945.1:p.Gly271Val
ENST00000682727.1:c.812G>T	ENSP00000507393.1:p.Gly271Val
ENST00000682876.1:c.941G>T	ENSP00000508389.1:p.Gly314Val
ENST00000683098.1:c.803+2766G>T	ENSP00000507670.1:n.803+2766G>T
ENST00000683258.1:c.*533G>T	ENSP00000507448.1:n.*533G>T
ENST00000683339.1:c.596G>T	ENSP00000507758.1:p.Gly199Val
ENST00000683403.1:c.812G>T	ENSP00000507896.1:p.Gly271Val
ENST00000683429.1:c.419G>T	ENSP00000507697.1:p.Gly140Val
ENST00000683665.1:c.812G>T	ENSP00000507068.1:p.Gly271Val
ENST00000683789.1:c.698G>T	ENSP00000507012.1:p.Gly233Val
ENST00000683847.1:n.656G>T
ENST00000683882.1:c.812G>T	ENSP00000506735.1:p.Gly271Val
ENST00000684024.1:c.*483G>T	ENSP00000507175.1:n.*483G>T
ENST00000684254.1:c.*538G>T	ENSP00000508001.1:n.*538G>T
ENST00000684310.1:c.74G>T	ENSP00000507550.1:p.Gly25Val
ENST00000684530.1:c.74G>T	ENSP00000507439.1:p.Gly25Val
ENST00000684652.1:n.1814G>T
ENST00000340941.11:c.812G>T MANE Select	ENSP00000343657.6:p.Gly271Val
ENST00000340941.10:c.812G>T	ENSP00000343657.6:p.Gly271Val
ENST00000505435.3:n.163G>T
ENST00000505787.7:n.626G>T
ENST00000509358.6:c.812G>T	ENSP00000420994.2:p.Gly271Val
ENST00000509539.2:c.137G>T	ENSP00000425474.2:p.Gly46Val
ENST00000510895.6:n.426G>T
ENST00000512218.6:c.698G>T	ENSP00000423202.2:p.Gly233Val
ENST00000629193.2:c.698G>T	ENSP00000486535.1:p.Gly233Val
NM_022132.4:c.812G>T	NP_071415.1:p.Gly271Val
XM_005248567.1:c.698G>T	XP_005248624.1:p.Gly233Val
XM_011543528.1:c.812G>T	XP_011541830.1:p.Gly271Val
XM_011543529.1:c.812G>T	XP_011541831.1:p.Gly271Val
NM_001363147.1:c.698G>T	NP_001350076.1:p.Gly233Val
XM_011543529.2:c.812G>T	XP_011541831.1:p.Gly271Val
XM_017009688.1:c.812G>T	XP_016865177.1:p.Gly271Val
XR_001742172.1:n.852G>T
NM_022132.5:c.812G>T MANE Select	NP_071415.1:p.Gly271Val