Canonical Allele Identifier: CA359987681

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70931027A>C (hg19) ; chr5:g.71635200A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635200A>C , CM000667.2:g.71635200A>C	GRCh38
NC_000005.9:g.70931027A>C , CM000667.1:g.70931027A>C	GRCh37
NC_000005.8:g.70966783A>C	NCBI36
NG_008882.1:g.52913A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.909A>C
ENST00000505787.8:n.2793A>C
ENST00000509358.7:c.953A>C	ENSP00000420994.3:p.Tyr318Ser
ENST00000509539.3:c.215A>C	ENSP00000425474.3:p.Tyr72Ser
ENST00000510895.7:n.1076A>C
ENST00000629193.3:c.839A>C	ENSP00000486535.2:p.Tyr280Ser
ENST00000681968.1:c.446A>C	ENSP00000508143.1:p.Tyr149Ser
ENST00000682045.1:c.809A>C	ENSP00000507329.1:p.Tyr270Ser
ENST00000682214.1:c.560A>C	ENSP00000507336.1:p.Tyr187Ser
ENST00000682499.1:n.1774A>C
ENST00000682541.1:c.953A>C	ENSP00000507673.1:p.Tyr318Ser
ENST00000682687.1:c.953A>C	ENSP00000507945.1:p.Tyr318Ser
ENST00000682727.1:c.953A>C	ENSP00000507393.1:p.Tyr318Ser
ENST00000682876.1:c.1082A>C	ENSP00000508389.1:p.Tyr361Ser
ENST00000683098.1:c.803+3015A>C	ENSP00000507670.1:n.803+3015A>C
ENST00000683258.1:c.*674A>C	ENSP00000507448.1:n.*674A>C
ENST00000683339.1:c.737A>C	ENSP00000507758.1:p.Tyr246Ser
ENST00000683403.1:c.863A>C	ENSP00000507896.1:p.Tyr288Ser
ENST00000683429.1:c.560A>C	ENSP00000507697.1:p.Tyr187Ser
ENST00000683665.1:c.953A>C	ENSP00000507068.1:p.Tyr318Ser
ENST00000683789.1:c.839A>C	ENSP00000507012.1:p.Tyr280Ser
ENST00000683847.1:n.797A>C
ENST00000683882.1:c.953A>C	ENSP00000506735.1:p.Tyr318Ser
ENST00000684024.1:c.*624A>C	ENSP00000507175.1:n.*624A>C
ENST00000684254.1:c.*679A>C	ENSP00000508001.1:n.*679A>C
ENST00000684310.1:c.165+158A>C	ENSP00000507550.1:n.165+158A>C
ENST00000684530.1:c.215A>C	ENSP00000507439.1:p.Tyr72Ser
ENST00000684652.1:n.1955A>C
ENST00000340941.11:c.953A>C MANE Select	ENSP00000343657.6:p.Tyr318Ser
ENST00000340941.10:c.953A>C	ENSP00000343657.6:p.Tyr318Ser
ENST00000505435.3:n.304A>C
ENST00000509358.6:c.953A>C	ENSP00000420994.2:p.Tyr318Ser
ENST00000509539.2:c.278A>C	ENSP00000425474.2:p.Tyr93Ser
ENST00000510895.6:n.567A>C
ENST00000512218.6:c.839A>C	ENSP00000423202.2:p.Tyr280Ser
ENST00000629193.2:c.839A>C	ENSP00000486535.1:p.Tyr280Ser
NM_022132.4:c.953A>C	NP_071415.1:p.Tyr318Ser
XM_005248567.1:c.839A>C	XP_005248624.1:p.Tyr280Ser
XM_011543528.1:c.953A>C	XP_011541830.1:p.Tyr318Ser
XM_011543529.1:c.953A>C	XP_011541831.1:p.Tyr318Ser
NM_001363147.1:c.839A>C	NP_001350076.1:p.Tyr280Ser
XM_011543529.2:c.953A>C	XP_011541831.1:p.Tyr318Ser
XM_017009688.1:c.953A>C	XP_016865177.1:p.Tyr318Ser
XR_001742172.1:n.993A>C
NM_022132.5:c.953A>C MANE Select	NP_071415.1:p.Tyr318Ser