Canonical Allele Identifier: CA359987392

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930982C>G (hg19) ; chr5:g.71635155C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635155C>G , CM000667.2:g.71635155C>G	GRCh38
NC_000005.9:g.70930982C>G , CM000667.1:g.70930982C>G	GRCh37
NC_000005.8:g.70966738C>G	NCBI36
NG_008882.1:g.52868C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.864C>G
ENST00000505787.8:n.2748C>G
ENST00000509358.7:c.908C>G	ENSP00000420994.3:p.Thr303Ser
ENST00000509539.3:c.170C>G	ENSP00000425474.3:p.Thr57Ser
ENST00000510895.7:n.1031C>G
ENST00000629193.3:c.794C>G	ENSP00000486535.2:p.Thr265Ser
ENST00000681968.1:c.401C>G	ENSP00000508143.1:p.Thr134Ser
ENST00000682045.1:c.764C>G	ENSP00000507329.1:p.Thr255Ser
ENST00000682214.1:c.515C>G	ENSP00000507336.1:p.Thr172Ser
ENST00000682499.1:n.1729C>G
ENST00000682541.1:c.908C>G	ENSP00000507673.1:p.Thr303Ser
ENST00000682687.1:c.908C>G	ENSP00000507945.1:p.Thr303Ser
ENST00000682727.1:c.908C>G	ENSP00000507393.1:p.Thr303Ser
ENST00000682876.1:c.1037C>G	ENSP00000508389.1:p.Thr346Ser
ENST00000683098.1:c.803+2970C>G	ENSP00000507670.1:n.803+2970C>G
ENST00000683258.1:c.*629C>G	ENSP00000507448.1:n.*629C>G
ENST00000683339.1:c.692C>G	ENSP00000507758.1:p.Thr231Ser
ENST00000683403.1:c.818C>G	ENSP00000507896.1:p.Thr273Ser
ENST00000683429.1:c.515C>G	ENSP00000507697.1:p.Thr172Ser
ENST00000683665.1:c.908C>G	ENSP00000507068.1:p.Thr303Ser
ENST00000683789.1:c.794C>G	ENSP00000507012.1:p.Thr265Ser
ENST00000683847.1:n.752C>G
ENST00000683882.1:c.908C>G	ENSP00000506735.1:p.Thr303Ser
ENST00000684024.1:c.*579C>G	ENSP00000507175.1:n.*579C>G
ENST00000684254.1:c.*634C>G	ENSP00000508001.1:n.*634C>G
ENST00000684310.1:c.165+113C>G	ENSP00000507550.1:n.165+113C>G
ENST00000684530.1:c.170C>G	ENSP00000507439.1:p.Thr57Ser
ENST00000684652.1:n.1910C>G
ENST00000340941.11:c.908C>G MANE Select	ENSP00000343657.6:p.Thr303Ser
ENST00000340941.10:c.908C>G	ENSP00000343657.6:p.Thr303Ser
ENST00000505435.3:n.259C>G
ENST00000509358.6:c.908C>G	ENSP00000420994.2:p.Thr303Ser
ENST00000509539.2:c.233C>G	ENSP00000425474.2:p.Thr78Ser
ENST00000510895.6:n.522C>G
ENST00000512218.6:c.794C>G	ENSP00000423202.2:p.Thr265Ser
ENST00000629193.2:c.794C>G	ENSP00000486535.1:p.Thr265Ser
NM_022132.4:c.908C>G	NP_071415.1:p.Thr303Ser
XM_005248567.1:c.794C>G	XP_005248624.1:p.Thr265Ser
XM_011543528.1:c.908C>G	XP_011541830.1:p.Thr303Ser
XM_011543529.1:c.908C>G	XP_011541831.1:p.Thr303Ser
NM_001363147.1:c.794C>G	NP_001350076.1:p.Thr265Ser
XM_011543529.2:c.908C>G	XP_011541831.1:p.Thr303Ser
XM_017009688.1:c.908C>G	XP_016865177.1:p.Thr303Ser
XR_001742172.1:n.948C>G
NM_022132.5:c.908C>G MANE Select	NP_071415.1:p.Thr303Ser