Canonical Allele Identifier: CA359986690

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930820A>T (hg19) ; chr5:g.71634993A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634993A>T , CM000667.2:g.71634993A>T	GRCh38
NC_000005.9:g.70930820A>T , CM000667.1:g.70930820A>T	GRCh37
NC_000005.8:g.70966576A>T	NCBI36
NG_008882.1:g.52706A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.810A>T
ENST00000505787.8:n.2694A>T
ENST00000509358.7:c.854A>T	ENSP00000420994.3:p.His285Leu
ENST00000509539.3:c.116A>T	ENSP00000425474.3:p.His39Leu
ENST00000510895.7:n.977A>T
ENST00000629193.3:c.740A>T	ENSP00000486535.2:p.His247Leu
ENST00000681968.1:c.347A>T	ENSP00000508143.1:p.His116Leu
ENST00000682045.1:c.710A>T	ENSP00000507329.1:p.His237Leu
ENST00000682214.1:c.461A>T	ENSP00000507336.1:p.His154Leu
ENST00000682499.1:n.1675A>T
ENST00000682541.1:c.854A>T	ENSP00000507673.1:p.His285Leu
ENST00000682687.1:c.854A>T	ENSP00000507945.1:p.His285Leu
ENST00000682727.1:c.854A>T	ENSP00000507393.1:p.His285Leu
ENST00000682876.1:c.983A>T	ENSP00000508389.1:p.His328Leu
ENST00000683098.1:c.803+2808A>T	ENSP00000507670.1:n.803+2808A>T
ENST00000683258.1:c.*575A>T	ENSP00000507448.1:n.*575A>T
ENST00000683339.1:c.638A>T	ENSP00000507758.1:p.His213Leu
ENST00000683403.1:c.813+41A>T	ENSP00000507896.1:n.813+41A>T
ENST00000683429.1:c.461A>T	ENSP00000507697.1:p.His154Leu
ENST00000683665.1:c.854A>T	ENSP00000507068.1:p.His285Leu
ENST00000683789.1:c.740A>T	ENSP00000507012.1:p.His247Leu
ENST00000683847.1:n.698A>T
ENST00000683882.1:c.854A>T	ENSP00000506735.1:p.His285Leu
ENST00000684024.1:c.*525A>T	ENSP00000507175.1:n.*525A>T
ENST00000684254.1:c.*580A>T	ENSP00000508001.1:n.*580A>T
ENST00000684310.1:c.116A>T	ENSP00000507550.1:p.His39Leu
ENST00000684530.1:c.116A>T	ENSP00000507439.1:p.His39Leu
ENST00000684652.1:n.1856A>T
ENST00000340941.11:c.854A>T MANE Select	ENSP00000343657.6:p.His285Leu
ENST00000340941.10:c.854A>T	ENSP00000343657.6:p.His285Leu
ENST00000505435.3:n.205A>T
ENST00000505787.7:n.668A>T
ENST00000509358.6:c.854A>T	ENSP00000420994.2:p.His285Leu
ENST00000509539.2:c.179A>T	ENSP00000425474.2:p.His60Leu
ENST00000510895.6:n.468A>T
ENST00000512218.6:c.740A>T	ENSP00000423202.2:p.His247Leu
ENST00000629193.2:c.740A>T	ENSP00000486535.1:p.His247Leu
NM_022132.4:c.854A>T	NP_071415.1:p.His285Leu
XM_005248567.1:c.740A>T	XP_005248624.1:p.His247Leu
XM_011543528.1:c.854A>T	XP_011541830.1:p.His285Leu
XM_011543529.1:c.854A>T	XP_011541831.1:p.His285Leu
NM_001363147.1:c.740A>T	NP_001350076.1:p.His247Leu
XM_011543529.2:c.854A>T	XP_011541831.1:p.His285Leu
XM_017009688.1:c.854A>T	XP_016865177.1:p.His285Leu
XR_001742172.1:n.894A>T
NM_022132.5:c.854A>T MANE Select	NP_071415.1:p.His285Leu