Canonical Allele Identifier: CA2578331518

Gene: MCCC2

Linked Data

• gnomAD v4: 5-71635065-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635065T>A , CM000667.2:g.71635065T>A	GRCh38
NC_000005.9:g.70930892T>A , CM000667.1:g.70930892T>A	GRCh37
NC_000005.8:g.70966648T>A	NCBI36
NG_008882.1:g.52778T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.859+23T>A
ENST00000505787.8:n.2743+23T>A
ENST00000509358.7:c.903+23T>A	ENSP00000420994.3:n.903+23T>A
ENST00000509539.3:c.165+23T>A	ENSP00000425474.3:n.165+23T>A
ENST00000510895.7:n.1026+23T>A
ENST00000629193.3:c.789+23T>A	ENSP00000486535.2:n.789+23T>A
ENST00000681968.1:c.396+23T>A	ENSP00000508143.1:n.396+23T>A
ENST00000682045.1:c.759+23T>A	ENSP00000507329.1:n.759+23T>A
ENST00000682214.1:c.510+23T>A	ENSP00000507336.1:n.510+23T>A
ENST00000682499.1:n.1724+23T>A
ENST00000682541.1:c.903+23T>A	ENSP00000507673.1:n.903+23T>A
ENST00000682687.1:c.903+23T>A	ENSP00000507945.1:n.903+23T>A
ENST00000682727.1:c.903+23T>A	ENSP00000507393.1:n.903+23T>A
ENST00000682876.1:c.1032+23T>A	ENSP00000508389.1:n.1032+23T>A
ENST00000683098.1:c.803+2880T>A	ENSP00000507670.1:n.803+2880T>A
ENST00000683258.1:c.*624+23T>A	ENSP00000507448.1:n.*624+23T>A
ENST00000683339.1:c.687+23T>A	ENSP00000507758.1:n.687+23T>A
ENST00000683403.1:c.814-86T>A	ENSP00000507896.1:n.814-86T>A
ENST00000683429.1:c.510+23T>A	ENSP00000507697.1:n.510+23T>A
ENST00000683665.1:c.903+23T>A	ENSP00000507068.1:n.903+23T>A
ENST00000683789.1:c.789+23T>A	ENSP00000507012.1:n.789+23T>A
ENST00000683847.1:n.747+23T>A
ENST00000683882.1:c.903+23T>A	ENSP00000506735.1:n.903+23T>A
ENST00000684024.1:c.*574+23T>A	ENSP00000507175.1:n.*574+23T>A
ENST00000684254.1:c.*629+23T>A	ENSP00000508001.1:n.*629+23T>A
ENST00000684310.1:c.165+23T>A	ENSP00000507550.1:n.165+23T>A
ENST00000684530.1:c.165+23T>A	ENSP00000507439.1:n.165+23T>A
ENST00000684652.1:n.1905+23T>A
ENST00000340941.11:c.903+23T>A MANE Select	ENSP00000343657.6:n.903+23T>A
ENST00000340941.10:c.903+23T>A	ENSP00000343657.6:n.903+23T>A
ENST00000505435.3:n.254+23T>A
ENST00000505787.7:n.740T>A
ENST00000509358.6:c.903+23T>A	ENSP00000420994.2:n.903+23T>A
ENST00000509539.2:c.228+23T>A	ENSP00000425474.2:n.228+23T>A
ENST00000510895.6:n.517+23T>A
ENST00000512218.6:c.789+23T>A	ENSP00000423202.2:n.789+23T>A
ENST00000629193.2:c.789+23T>A	ENSP00000486535.1:n.789+23T>A
NM_022132.4:c.903+23T>A	NP_071415.1:n.903+23T>A
XM_005248567.1:c.789+23T>A	XP_005248624.1:n.789+23T>A
XM_011543528.1:c.903+23T>A	XP_011541830.1:n.903+23T>A
XM_011543529.1:c.903+23T>A	XP_011541831.1:n.903+23T>A
NM_001363147.1:c.789+23T>A	NP_001350076.1:n.789+23T>A
XM_011543529.2:c.903+23T>A	XP_011541831.1:n.903+23T>A
XM_017009688.1:c.903+23T>A	XP_016865177.1:n.903+23T>A
XR_001742172.1:n.943+23T>A
NM_022132.5:c.903+23T>A MANE Select	NP_071415.1:n.903+23T>A