Canonical Allele Identifier: CA2674882406

Gene: MCC

Linked Data

• gnomAD v4: 5-113064167-C-CCTATGTGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113064169_113064176dup , CM000667.2:g.113064169_113064176dup	GRCh38
NC_000005.9:g.112399866_112399873dup , CM000667.1:g.112399866_112399873dup	GRCh37
NC_000005.8:g.112427765_112427772dup	NCBI36
NG_012265.1:g.429656_429663dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302475.9:c.1460-8_1460-1dup	ENSP00000305617.4:n.1460-8_1460-1dup
ENST00000408903.7:c.2030-8_2030-1dup MANE Select	ENSP00000386227.3:n.2030-8_2030-1dup
ENST00000302475.8:c.1460-8_1460-1dup	ENSP00000305617.4:n.1460-8_1460-1dup
ENST00000408903.6:c.2030-8_2030-1dup	ENSP00000386227.3:n.2030-8_2030-1dup
ENST00000514701.5:c.1460-8_1460-1dup	ENSP00000485220.1:n.1460-8_1460-1dup
ENST00000515367.6:c.1271-8_1271-1dup	ENSP00000421615.2:n.1271-8_1271-1dup
NM_001085377.1:c.2030-8_2030-1dup	NP_001078846.1:n.2030-8_2030-1dup
NM_002387.2:c.1460-8_1460-1dup	NP_002378.1:n.1460-8_1460-1dup
XM_005271991.2:c.1460-8_1460-1dup	XP_005272048.1:n.1460-8_1460-1dup
XM_005271991.3:c.1460-8_1460-1dup	XP_005272048.1:n.1460-8_1460-1dup
XM_017009473.1:c.2030-8_2030-1dup	XP_016864962.1:n.2030-8_2030-1dup
XM_017009474.1:c.1430-8_1430-1dup	XP_016864963.1:n.1430-8_1430-1dup
XM_024446049.1:c.1271-8_1271-1dup	XP_024301817.1:n.1271-8_1271-1dup
XM_024446050.1:c.1271-8_1271-1dup	XP_024301818.1:n.1271-8_1271-1dup
XM_024446051.1:c.1271-8_1271-1dup	XP_024301819.1:n.1271-8_1271-1dup
XM_024446052.1:c.1271-8_1271-1dup	XP_024301820.1:n.1271-8_1271-1dup
NM_001085377.2:c.2030-8_2030-1dup MANE Select	NP_001078846.2:n.2030-8_2030-1dup
NM_002387.3:c.1460-8_1460-1dup	NP_002378.2:n.1460-8_1460-1dup