Canonical Allele Identifier: CA2552346968
Gene: MCC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387944del , CM000667.2:g.113387944del GRCh38
NC_000005.9:g.112723641del , CM000667.1:g.112723641del GRCh37
NC_000005.8:g.112751540del NCBI36
NG_012265.1:g.105890del

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2729del MANE Select ENSP00000386227.3:n.171-2729del
ENST00000408903.6:c.171-2729del ENSP00000386227.3:n.171-2729del
NM_001085377.1:c.171-2729del NP_001078846.1:n.171-2729del
XM_017009473.1:c.171-2729del XP_016864962.1:n.171-2729del
NM_001085377.2:c.171-2729del MANE Select NP_001078846.2:n.171-2729del
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