Canonical Allele Identifier: CA359987665

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70931023T>G (hg19) ; chr5:g.71635196T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635196T>G , CM000667.2:g.71635196T>G	GRCh38
NC_000005.9:g.70931023T>G , CM000667.1:g.70931023T>G	GRCh37
NC_000005.8:g.70966779T>G	NCBI36
NG_008882.1:g.52909T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.905T>G
ENST00000505787.8:n.2789T>G
ENST00000509358.7:c.949T>G	ENSP00000420994.3:p.Leu317Val
ENST00000509539.3:c.211T>G	ENSP00000425474.3:p.Leu71Val
ENST00000510895.7:n.1072T>G
ENST00000629193.3:c.835T>G	ENSP00000486535.2:p.Leu279Val
ENST00000681968.1:c.442T>G	ENSP00000508143.1:p.Leu148Val
ENST00000682045.1:c.805T>G	ENSP00000507329.1:p.Leu269Val
ENST00000682214.1:c.556T>G	ENSP00000507336.1:p.Leu186Val
ENST00000682499.1:n.1770T>G
ENST00000682541.1:c.949T>G	ENSP00000507673.1:p.Leu317Val
ENST00000682687.1:c.949T>G	ENSP00000507945.1:p.Leu317Val
ENST00000682727.1:c.949T>G	ENSP00000507393.1:p.Leu317Val
ENST00000682876.1:c.1078T>G	ENSP00000508389.1:p.Leu360Val
ENST00000683098.1:c.803+3011T>G	ENSP00000507670.1:n.803+3011T>G
ENST00000683258.1:c.*670T>G	ENSP00000507448.1:n.*670T>G
ENST00000683339.1:c.733T>G	ENSP00000507758.1:p.Leu245Val
ENST00000683403.1:c.859T>G	ENSP00000507896.1:p.Leu287Val
ENST00000683429.1:c.556T>G	ENSP00000507697.1:p.Leu186Val
ENST00000683665.1:c.949T>G	ENSP00000507068.1:p.Leu317Val
ENST00000683789.1:c.835T>G	ENSP00000507012.1:p.Leu279Val
ENST00000683847.1:n.793T>G
ENST00000683882.1:c.949T>G	ENSP00000506735.1:p.Leu317Val
ENST00000684024.1:c.*620T>G	ENSP00000507175.1:n.*620T>G
ENST00000684254.1:c.*675T>G	ENSP00000508001.1:n.*675T>G
ENST00000684310.1:c.165+154T>G	ENSP00000507550.1:n.165+154T>G
ENST00000684530.1:c.211T>G	ENSP00000507439.1:p.Leu71Val
ENST00000684652.1:n.1951T>G
ENST00000340941.11:c.949T>G MANE Select	ENSP00000343657.6:p.Leu317Val
ENST00000340941.10:c.949T>G	ENSP00000343657.6:p.Leu317Val
ENST00000505435.3:n.300T>G
ENST00000509358.6:c.949T>G	ENSP00000420994.2:p.Leu317Val
ENST00000509539.2:c.274T>G	ENSP00000425474.2:p.Leu92Val
ENST00000510895.6:n.563T>G
ENST00000512218.6:c.835T>G	ENSP00000423202.2:p.Leu279Val
ENST00000629193.2:c.835T>G	ENSP00000486535.1:p.Leu279Val
NM_022132.4:c.949T>G	NP_071415.1:p.Leu317Val
XM_005248567.1:c.835T>G	XP_005248624.1:p.Leu279Val
XM_011543528.1:c.949T>G	XP_011541830.1:p.Leu317Val
XM_011543529.1:c.949T>G	XP_011541831.1:p.Leu317Val
NM_001363147.1:c.835T>G	NP_001350076.1:p.Leu279Val
XM_011543529.2:c.949T>G	XP_011541831.1:p.Leu317Val
XM_017009688.1:c.949T>G	XP_016865177.1:p.Leu317Val
XR_001742172.1:n.989T>G
NM_022132.5:c.949T>G MANE Select	NP_071415.1:p.Leu317Val