Canonical Allele Identifier: CA360626215
Gene: MCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113064086T>C , CM000667.2:g.113064086T>C GRCh38
NC_000005.9:g.112399783T>C , CM000667.1:g.112399783T>C GRCh37
NC_000005.8:g.112427682T>C NCBI36
NG_012265.1:g.429745A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000302475.9:c.1541A>G ENSP00000305617.4:p.Lys514Arg
ENST00000408903.7:c.2111A>G MANE Select ENSP00000386227.3:p.Lys704Arg
ENST00000302475.8:c.1541A>G ENSP00000305617.4:p.Lys514Arg
ENST00000408903.6:c.2111A>G ENSP00000386227.3:p.Lys704Arg
ENST00000514701.5:c.1541A>G ENSP00000485220.1:p.Lys514Arg
ENST00000515367.6:c.1352A>G ENSP00000421615.2:p.Lys451Arg
NM_001085377.1:c.2111A>G NP_001078846.1:p.Lys704Arg
NM_002387.2:c.1541A>G NP_002378.1:p.Lys514Arg
XM_005271991.2:c.1541A>G XP_005272048.1:p.Lys514Arg
XM_005271991.3:c.1541A>G XP_005272048.1:p.Lys514Arg
XM_017009473.1:c.2111A>G XP_016864962.1:p.Lys704Arg
XM_017009474.1:c.1511A>G XP_016864963.1:p.Lys504Arg
XM_024446049.1:c.1352A>G XP_024301817.1:p.Lys451Arg
XM_024446050.1:c.1352A>G XP_024301818.1:p.Lys451Arg
XM_024446051.1:c.1352A>G XP_024301819.1:p.Lys451Arg
XM_024446052.1:c.1352A>G XP_024301820.1:p.Lys451Arg
NM_001085377.2:c.2111A>G MANE Select NP_001078846.2:p.Lys704Arg
NM_002387.3:c.1541A>G NP_002378.2:p.Lys514Arg