Canonical Allele Identifier: CA360626099
Gene: MCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064027T>A , CM000667.2:g.113064027T>A GRCh38
NC_000005.9:g.112399724T>A , CM000667.1:g.112399724T>A GRCh37
NC_000005.8:g.112427623T>A NCBI36
NG_012265.1:g.429804A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302475.9:c.1600A>T ENSP00000305617.4:p.Ser534Cys
ENST00000408903.7:c.2170A>T MANE Select ENSP00000386227.3:p.Ser724Cys
ENST00000302475.8:c.1600A>T ENSP00000305617.4:p.Ser534Cys
ENST00000408903.6:c.2170A>T ENSP00000386227.3:p.Ser724Cys
ENST00000514701.5:c.1600A>T ENSP00000485220.1:p.Ser534Cys
ENST00000515367.6:c.1411A>T ENSP00000421615.2:p.Ser471Cys
ENST00000624689.3:c.14A>T
NM_001085377.1:c.2170A>T NP_001078846.1:p.Ser724Cys
NM_002387.2:c.1600A>T NP_002378.1:p.Ser534Cys
XM_005271991.2:c.1600A>T XP_005272048.1:p.Ser534Cys
XM_005271991.3:c.1600A>T XP_005272048.1:p.Ser534Cys
XM_017009473.1:c.2170A>T XP_016864962.1:p.Ser724Cys
XM_017009474.1:c.1570A>T XP_016864963.1:p.Ser524Cys
XM_024446049.1:c.1411A>T XP_024301817.1:p.Ser471Cys
XM_024446050.1:c.1411A>T XP_024301818.1:p.Ser471Cys
XM_024446051.1:c.1411A>T XP_024301819.1:p.Ser471Cys
XM_024446052.1:c.1411A>T XP_024301820.1:p.Ser471Cys
NM_001085377.2:c.2170A>T MANE Select NP_001078846.2:p.Ser724Cys
NM_002387.3:c.1600A>T NP_002378.2:p.Ser534Cys