Canonical Allele Identifier: CA2674882405
Gene: MCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064155_113064176dup , CM000667.2:g.113064155_113064176dup GRCh38
NC_000005.9:g.112399852_112399873dup , CM000667.1:g.112399852_112399873dup GRCh37
NC_000005.8:g.112427751_112427772dup NCBI36
NG_012265.1:g.429656_429677dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000302475.9:c.1460-8_1473dup
ENST00000408903.7:c.2030-8_2043dup
ENST00000302475.8:c.1460-8_1473dup
ENST00000408903.6:c.2030-8_2043dup
ENST00000514701.5:c.1460-8_1473dup
ENST00000515367.6:c.1271-8_1284dup
NM_001085377.1:c.2030-8_2043dup
NM_002387.2:c.1460-8_1473dup
XM_005271991.2:c.1460-8_1473dup
XM_005271991.3:c.1460-8_1473dup
XM_017009473.1:c.2030-8_2043dup
XM_017009474.1:c.1430-8_1443dup
XM_024446049.1:c.1271-8_1284dup
XM_024446050.1:c.1271-8_1284dup
XM_024446051.1:c.1271-8_1284dup
XM_024446052.1:c.1271-8_1284dup
NM_001085377.2:c.2030-8_2043dup
NM_002387.3:c.1460-8_1473dup