Canonical Allele Identifier: CA2536240395

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635108A>C , CM000667.2:g.71635108A>C	GRCh38
NC_000005.9:g.70930935A>C , CM000667.1:g.70930935A>C	GRCh37
NC_000005.8:g.70966691A>C	NCBI36
NG_008882.1:g.52821A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.860-43A>C
ENST00000505787.8:n.2744-43A>C
ENST00000509358.7:c.904-43A>C	ENSP00000420994.3:n.904-43A>C
ENST00000509539.3:c.166-43A>C	ENSP00000425474.3:n.166-43A>C
ENST00000510895.7:n.1027-43A>C
ENST00000629193.3:c.790-43A>C	ENSP00000486535.2:n.790-43A>C
ENST00000681968.1:c.397-43A>C	ENSP00000508143.1:n.397-43A>C
ENST00000682045.1:c.760-43A>C	ENSP00000507329.1:n.760-43A>C
ENST00000682214.1:c.511-43A>C	ENSP00000507336.1:n.511-43A>C
ENST00000682499.1:n.1725-43A>C
ENST00000682541.1:c.904-43A>C	ENSP00000507673.1:n.904-43A>C
ENST00000682687.1:c.904-43A>C	ENSP00000507945.1:n.904-43A>C
ENST00000682727.1:c.904-43A>C	ENSP00000507393.1:n.904-43A>C
ENST00000682876.1:c.1033-43A>C	ENSP00000508389.1:n.1033-43A>C
ENST00000683098.1:c.803+2923A>C	ENSP00000507670.1:n.803+2923A>C
ENST00000683258.1:c.*625-43A>C	ENSP00000507448.1:n.*625-43A>C
ENST00000683339.1:c.688-43A>C	ENSP00000507758.1:n.688-43A>C
ENST00000683403.1:c.814-43A>C	ENSP00000507896.1:n.814-43A>C
ENST00000683429.1:c.511-43A>C	ENSP00000507697.1:n.511-43A>C
ENST00000683665.1:c.904-43A>C	ENSP00000507068.1:n.904-43A>C
ENST00000683789.1:c.790-43A>C	ENSP00000507012.1:n.790-43A>C
ENST00000683847.1:n.748-43A>C
ENST00000683882.1:c.904-43A>C	ENSP00000506735.1:n.904-43A>C
ENST00000684024.1:c.*575-43A>C	ENSP00000507175.1:n.*575-43A>C
ENST00000684254.1:c.*630-43A>C	ENSP00000508001.1:n.*630-43A>C
ENST00000684310.1:c.165+66A>C	ENSP00000507550.1:n.165+66A>C
ENST00000684530.1:c.166-43A>C	ENSP00000507439.1:n.166-43A>C
ENST00000684652.1:n.1906-43A>C
ENST00000340941.11:c.904-43A>C MANE Select	ENSP00000343657.6:n.904-43A>C
ENST00000340941.10:c.904-43A>C	ENSP00000343657.6:n.904-43A>C
ENST00000505435.3:n.255-43A>C
ENST00000509358.6:c.904-43A>C	ENSP00000420994.2:n.904-43A>C
ENST00000509539.2:c.229-43A>C	ENSP00000425474.2:n.229-43A>C
ENST00000510895.6:n.518-43A>C
ENST00000512218.6:c.790-43A>C	ENSP00000423202.2:n.790-43A>C
ENST00000629193.2:c.790-43A>C	ENSP00000486535.1:n.790-43A>C
NM_022132.4:c.904-43A>C	NP_071415.1:n.904-43A>C
XM_005248567.1:c.790-43A>C	XP_005248624.1:n.790-43A>C
XM_011543528.1:c.904-43A>C	XP_011541830.1:n.904-43A>C
XM_011543529.1:c.904-43A>C	XP_011541831.1:n.904-43A>C
NM_001363147.1:c.790-43A>C	NP_001350076.1:n.790-43A>C
XM_011543529.2:c.904-43A>C	XP_011541831.1:n.904-43A>C
XM_017009688.1:c.904-43A>C	XP_016865177.1:n.904-43A>C
XR_001742172.1:n.944-43A>C
NM_022132.5:c.904-43A>C MANE Select	NP_071415.1:n.904-43A>C