Canonical Allele Identifier: CA1554387763

Gene: MCCC2

Linked Data

• dbSNP Id: rs1746871584

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635102_71635107del , CM000667.2:g.71635102_71635107del	GRCh38
NC_000005.9:g.70930929_70930934del , CM000667.1:g.70930929_70930934del	GRCh37
NC_000005.8:g.70966685_70966690del	NCBI36
NG_008882.1:g.52815_52820del

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.860-49_860-44del
ENST00000505787.8:n.2744-49_2744-44del
ENST00000509358.7:c.904-49_904-44del	ENSP00000420994.3:n.904-49_904-44del
ENST00000509539.3:c.166-49_166-44del	ENSP00000425474.3:n.166-49_166-44del
ENST00000510895.7:n.1027-49_1027-44del
ENST00000629193.3:c.790-49_790-44del	ENSP00000486535.2:n.790-49_790-44del
ENST00000681968.1:c.397-49_397-44del	ENSP00000508143.1:n.397-49_397-44del
ENST00000682045.1:c.760-49_760-44del	ENSP00000507329.1:n.760-49_760-44del
ENST00000682214.1:c.511-49_511-44del	ENSP00000507336.1:n.511-49_511-44del
ENST00000682499.1:n.1725-49_1725-44del
ENST00000682541.1:c.904-49_904-44del	ENSP00000507673.1:n.904-49_904-44del
ENST00000682687.1:c.904-49_904-44del	ENSP00000507945.1:n.904-49_904-44del
ENST00000682727.1:c.904-49_904-44del	ENSP00000507393.1:n.904-49_904-44del
ENST00000682876.1:c.1033-49_1033-44del	ENSP00000508389.1:n.1033-49_1033-44del
ENST00000683098.1:c.803+2917_803+2922del	ENSP00000507670.1:n.803+2917_803+2922del
ENST00000683258.1:c.*625-49_*625-44del	ENSP00000507448.1:n.*625-49_*625-44del
ENST00000683339.1:c.688-49_688-44del	ENSP00000507758.1:n.688-49_688-44del
ENST00000683403.1:c.814-49_814-44del	ENSP00000507896.1:n.814-49_814-44del
ENST00000683429.1:c.511-49_511-44del	ENSP00000507697.1:n.511-49_511-44del
ENST00000683665.1:c.904-49_904-44del	ENSP00000507068.1:n.904-49_904-44del
ENST00000683789.1:c.790-49_790-44del	ENSP00000507012.1:n.790-49_790-44del
ENST00000683847.1:n.748-49_748-44del
ENST00000683882.1:c.904-49_904-44del	ENSP00000506735.1:n.904-49_904-44del
ENST00000684024.1:c.*575-49_*575-44del	ENSP00000507175.1:n.*575-49_*575-44del
ENST00000684254.1:c.*630-49_*630-44del	ENSP00000508001.1:n.*630-49_*630-44del
ENST00000684310.1:c.165+60_165+65del	ENSP00000507550.1:n.165+60_165+65del
ENST00000684530.1:c.166-49_166-44del	ENSP00000507439.1:n.166-49_166-44del
ENST00000684652.1:n.1906-49_1906-44del
ENST00000340941.11:c.904-49_904-44del MANE Select	ENSP00000343657.6:n.904-49_904-44del
ENST00000340941.10:c.904-49_904-44del	ENSP00000343657.6:n.904-49_904-44del
ENST00000505435.3:n.255-49_255-44del
ENST00000509358.6:c.904-49_904-44del	ENSP00000420994.2:n.904-49_904-44del
ENST00000509539.2:c.229-49_229-44del	ENSP00000425474.2:n.229-49_229-44del
ENST00000510895.6:n.518-49_518-44del
ENST00000512218.6:c.790-49_790-44del	ENSP00000423202.2:n.790-49_790-44del
ENST00000629193.2:c.790-49_790-44del	ENSP00000486535.1:n.790-49_790-44del
NM_022132.4:c.904-49_904-44del	NP_071415.1:n.904-49_904-44del
XM_005248567.1:c.790-49_790-44del	XP_005248624.1:n.790-49_790-44del
XM_011543528.1:c.904-49_904-44del	XP_011541830.1:n.904-49_904-44del
XM_011543529.1:c.904-49_904-44del	XP_011541831.1:n.904-49_904-44del
NM_001363147.1:c.790-49_790-44del	NP_001350076.1:n.790-49_790-44del
XM_011543529.2:c.904-49_904-44del	XP_011541831.1:n.904-49_904-44del
XM_017009688.1:c.904-49_904-44del	XP_016865177.1:n.904-49_904-44del
XR_001742172.1:n.944-49_944-44del
NM_022132.5:c.904-49_904-44del MANE Select	NP_071415.1:n.904-49_904-44del