Canonical Allele Identifier: CA2710021732
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs2150229711

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064054del , CM000667.2:g.113064054del GRCh38
NC_000005.9:g.112399751del , CM000667.1:g.112399751del GRCh37
NC_000005.8:g.112427650del NCBI36
NG_012265.1:g.429781del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302475.9:c.1577del ENSP00000305617.4:p.Gly526GlufsTer?
ENST00000408903.7:c.2147del MANE Select ENSP00000386227.3:p.Gly716GlufsTer?
ENST00000302475.8:c.1577del ENSP00000305617.4:p.Gly526GlufsTer?
ENST00000408903.6:c.2147del ENSP00000386227.3:p.Gly716GlufsTer?
ENST00000514701.5:c.1577del ENSP00000485220.1:p.Gly526GlufsTer?
ENST00000515367.6:c.1388del ENSP00000421615.2:p.Gly463GlufsTer?
NM_001085377.1:c.2147del NP_001078846.1:p.Gly716GlufsTer?
NM_002387.2:c.1577del NP_002378.1:p.Gly526GlufsTer?
XM_005271991.2:c.1577del XP_005272048.1:p.Gly526GlufsTer?
XM_005271991.3:c.1577del XP_005272048.1:p.Gly526GlufsTer?
XM_017009473.1:c.2147del XP_016864962.1:p.Gly716GlufsTer?
XM_017009474.1:c.1547del XP_016864963.1:p.Gly516GlufsTer?
XM_024446049.1:c.1388del XP_024301817.1:p.Gly463GlufsTer?
XM_024446050.1:c.1388del XP_024301818.1:p.Gly463GlufsTer?
XM_024446051.1:c.1388del XP_024301819.1:p.Gly463GlufsTer?
XM_024446052.1:c.1388del XP_024301820.1:p.Gly463GlufsTer?
NM_001085377.2:c.2147del MANE Select NP_001078846.2:p.Gly716GlufsTer?
NM_002387.3:c.1577del NP_002378.2:p.Gly526GlufsTer?