Canonical Allele Identifier: CA2674882403
Gene: MCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064150_113064151insCC , CM000667.2:g.113064150_113064151insCC GRCh38
NC_000005.9:g.112399847_112399848insCC , CM000667.1:g.112399847_112399848insCC GRCh37
NC_000005.8:g.112427746_112427747insCC NCBI36
NG_012265.1:g.429681_429682insGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000302475.9:c.1477_1478insGG ENSP00000305617.4:p.Glu493GlyfsTer27
ENST00000408903.7:c.2047_2048insGG MANE Select ENSP00000386227.3:p.Glu683GlyfsTer27
ENST00000302475.8:c.1477_1478insGG ENSP00000305617.4:p.Glu493GlyfsTer27
ENST00000408903.6:c.2047_2048insGG ENSP00000386227.3:p.Glu683GlyfsTer27
ENST00000514701.5:c.1477_1478insGG ENSP00000485220.1:p.Glu493GlyfsTer27
ENST00000515367.6:c.1288_1289insGG ENSP00000421615.2:p.Glu430GlyfsTer27
NM_001085377.1:c.2047_2048insGG NP_001078846.1:p.Glu683GlyfsTer27
NM_002387.2:c.1477_1478insGG NP_002378.1:p.Glu493GlyfsTer27
XM_005271991.2:c.1477_1478insGG XP_005272048.1:p.Glu493GlyfsTer27
XM_005271991.3:c.1477_1478insGG XP_005272048.1:p.Glu493GlyfsTer27
XM_017009473.1:c.2047_2048insGG XP_016864962.1:p.Glu683GlyfsTer27
XM_017009474.1:c.1447_1448insGG XP_016864963.1:p.Glu483GlyfsTer27
XM_024446049.1:c.1288_1289insGG XP_024301817.1:p.Glu430GlyfsTer27
XM_024446050.1:c.1288_1289insGG XP_024301818.1:p.Glu430GlyfsTer27
XM_024446051.1:c.1288_1289insGG XP_024301819.1:p.Glu430GlyfsTer27
XM_024446052.1:c.1288_1289insGG XP_024301820.1:p.Glu430GlyfsTer27
NM_001085377.2:c.2047_2048insGG MANE Select NP_001078846.2:p.Glu683GlyfsTer27
NM_002387.3:c.1477_1478insGG NP_002378.2:p.Glu493GlyfsTer27