Canonical Allele Identifier: CA360002556

Gene: MCCC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71587555G>T , CM000667.2:g.71587555G>T	GRCh38
NC_000005.9:g.70883382G>T , CM000667.1:g.70883382G>T	GRCh37
NC_000005.8:g.70919138G>T	NCBI36
NG_008882.1:g.5268G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.199+1G>T
ENST00000505787.8:n.1969+3389G>T
ENST00000509358.7:c.129+1G>T	ENSP00000420994.3:n.129+1G>T
ENST00000510895.7:n.252+1G>T
ENST00000629193.3:c.129+1G>T	ENSP00000486535.2:n.129+1G>T
ENST00000681968.1:c.-265+113G>T	ENSP00000508143.1:n.-265+113G>T
ENST00000682045.1:c.-16+705G>T	ENSP00000507329.1:n.-16+705G>T
ENST00000682214.1:c.-198+705G>T	ENSP00000507336.1:n.-198+705G>T
ENST00000682499.1:n.950+4982G>T
ENST00000682541.1:c.129+1G>T	ENSP00000507673.1:n.129+1G>T
ENST00000682687.1:c.129+1G>T	ENSP00000507945.1:n.129+1G>T
ENST00000682727.1:c.129+1G>T	ENSP00000507393.1:n.129+1G>T
ENST00000682876.1:c.129+1G>T	ENSP00000508389.1:n.129+1G>T
ENST00000683098.1:c.129+1G>T	ENSP00000507670.1:n.129+1G>T
ENST00000683258.1:c.129+1G>T	ENSP00000507448.1:n.129+1G>T
ENST00000683339.1:c.129+1G>T	ENSP00000507758.1:n.129+1G>T
ENST00000683403.1:c.129+1G>T	ENSP00000507896.1:n.129+1G>T
ENST00000683429.1:c.-265+113G>T	ENSP00000507697.1:n.-265+113G>T
ENST00000683665.1:c.129+1G>T	ENSP00000507068.1:n.129+1G>T
ENST00000683789.1:c.129+1G>T	ENSP00000507012.1:n.129+1G>T
ENST00000683882.1:c.129+1G>T	ENSP00000506735.1:n.129+1G>T
ENST00000684024.1:c.129+1G>T	ENSP00000507175.1:n.129+1G>T
ENST00000684254.1:c.129+1G>T	ENSP00000508001.1:n.129+1G>T
ENST00000340941.11:c.129+1G>T MANE Select	ENSP00000343657.6:n.129+1G>T
ENST00000340941.10:c.129+1G>T	ENSP00000343657.6:n.129+1G>T
ENST00000509358.6:c.129+1G>T	ENSP00000420994.2:n.129+1G>T
ENST00000512218.6:c.129+1G>T	ENSP00000423202.2:n.129+1G>T
ENST00000629193.2:c.129+1G>T	ENSP00000486535.1:n.129+1G>T
NM_022132.4:c.129+1G>T	NP_071415.1:n.129+1G>T
XM_005248567.1:c.129+1G>T	XP_005248624.1:n.129+1G>T
XM_011543528.1:c.129+1G>T	XP_011541830.1:n.129+1G>T
XM_011543529.1:c.129+1G>T	XP_011541831.1:n.129+1G>T
NM_001363147.1:c.129+1G>T	NP_001350076.1:n.129+1G>T
XM_011543529.2:c.129+1G>T	XP_011541831.1:n.129+1G>T
XM_017009688.1:c.129+1G>T	XP_016865177.1:n.129+1G>T
XR_001742172.1:n.169+1G>T
NM_022132.5:c.129+1G>T MANE Select	NP_071415.1:n.129+1G>T