Canonical Allele Identifier: CA1573632494
Gene: MCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064013C= , CM000667.2:g.113064013C= GRCh38
NC_000005.9:g.112399710C= , CM000667.1:g.112399710C= GRCh37
NC_000005.8:g.112427609C= NCBI36
NG_012265.1:g.429818G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302475.9:c.1614G= ENSP00000305617.4:p.Trp538=
ENST00000408903.7:c.2184G= MANE Select ENSP00000386227.3:p.Trp728=
ENST00000302475.8:c.1614G= ENSP00000305617.4:p.Trp538=
ENST00000408903.6:c.2184G= ENSP00000386227.3:p.Trp728=
ENST00000514701.5:c.1614G= ENSP00000485220.1:p.Trp538=
ENST00000515367.6:c.1425G= ENSP00000421615.2:p.Trp475=
ENST00000624689.3:c.28G=
NM_001085377.1:c.2184G= NP_001078846.1:p.Trp728=
NM_002387.2:c.1614G= NP_002378.1:p.Trp538=
XM_005271991.2:c.1614G= XP_005272048.1:p.Trp538=
XM_005271991.3:c.1614G= XP_005272048.1:p.Trp538=
XM_017009473.1:c.2184G= XP_016864962.1:p.Trp728=
XM_017009474.1:c.1584G= XP_016864963.1:p.Trp528=
XM_024446049.1:c.1425G= XP_024301817.1:p.Trp475=
XM_024446050.1:c.1425G= XP_024301818.1:p.Trp475=
XM_024446051.1:c.1425G= XP_024301819.1:p.Trp475=
XM_024446052.1:c.1425G= XP_024301820.1:p.Trp475=
NM_001085377.2:c.2184G= MANE Select NP_001078846.2:p.Trp728=
NM_002387.3:c.1614G= NP_002378.2:p.Trp538=