Canonical Allele Identifier: CA360010879

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70898426T>G (hg19) ; chr5:g.71602599T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71602599T>G , CM000667.2:g.71602599T>G	GRCh38
NC_000005.9:g.70898426T>G , CM000667.1:g.70898426T>G	GRCh37
NC_000005.8:g.70934182T>G	NCBI36
NG_008882.1:g.20312T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.547T>G
ENST00000505787.8:n.2317T>G
ENST00000509358.7:c.477T>G	ENSP00000420994.3:p.Ile159Met
ENST00000510895.7:n.600T>G
ENST00000629193.3:c.477T>G	ENSP00000486535.2:p.Ile159Met
ENST00000681968.1:c.84T>G	ENSP00000508143.1:p.Ile28Met
ENST00000682045.1:c.333T>G	ENSP00000507329.1:p.Ile111Met
ENST00000682214.1:c.84T>G	ENSP00000507336.1:p.Ile28Met
ENST00000682499.1:n.1298T>G
ENST00000682541.1:c.477T>G	ENSP00000507673.1:p.Ile159Met
ENST00000682687.1:c.477T>G	ENSP00000507945.1:p.Ile159Met
ENST00000682727.1:c.477T>G	ENSP00000507393.1:p.Ile159Met
ENST00000682876.1:c.477T>G	ENSP00000508389.1:p.Ile159Met
ENST00000683098.1:c.477T>G	ENSP00000507670.1:p.Ile159Met
ENST00000683258.1:c.*198T>G	ENSP00000507448.1:n.*198T>G
ENST00000683339.1:c.375T>G	ENSP00000507758.1:p.Ile125Met
ENST00000683403.1:c.477T>G	ENSP00000507896.1:p.Ile159Met
ENST00000683429.1:c.84T>G	ENSP00000507697.1:p.Ile28Met
ENST00000683665.1:c.477T>G	ENSP00000507068.1:p.Ile159Met
ENST00000683789.1:c.477T>G	ENSP00000507012.1:p.Ile159Met
ENST00000683882.1:c.477T>G	ENSP00000506735.1:p.Ile159Met
ENST00000684024.1:c.*148T>G	ENSP00000507175.1:n.*148T>G
ENST00000684254.1:c.*203T>G	ENSP00000508001.1:n.*203T>G
ENST00000340941.11:c.477T>G MANE Select	ENSP00000343657.6:p.Ile159Met
ENST00000340941.10:c.477T>G	ENSP00000343657.6:p.Ile159Met
ENST00000505787.7:n.291T>G
ENST00000507169.5:n.403T>G
ENST00000509358.6:c.477T>G	ENSP00000420994.2:p.Ile159Met
ENST00000510895.6:n.91T>G
ENST00000512218.6:c.477T>G	ENSP00000423202.2:p.Ile159Met
ENST00000629193.2:c.477T>G	ENSP00000486535.1:p.Ile159Met
NM_022132.4:c.477T>G	NP_071415.1:p.Ile159Met
XM_005248567.1:c.477T>G	XP_005248624.1:p.Ile159Met
XM_011543528.1:c.477T>G	XP_011541830.1:p.Ile159Met
XM_011543529.1:c.477T>G	XP_011541831.1:p.Ile159Met
NM_001363147.1:c.477T>G	NP_001350076.1:p.Ile159Met
XM_011543529.2:c.477T>G	XP_011541831.1:p.Ile159Met
XM_017009688.1:c.477T>G	XP_016865177.1:p.Ile159Met
XR_001742172.1:n.517T>G
NM_022132.5:c.477T>G MANE Select	NP_071415.1:p.Ile159Met