Canonical Allele Identifier: CA1573788891
Gene: MCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387723_113387724delinsTA , CM000667.2:g.113387723_113387724delinsTA GRCh38
NC_000005.9:g.112723420_112723421delinsTA , CM000667.1:g.112723420_112723421delinsTA GRCh37
NC_000005.8:g.112751319_112751320delinsTA NCBI36
NG_012265.1:g.106107_106108delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2512_171-2511delinsTA MANE Select ENSP00000386227.3:n.171-2512_171-2511delinsTA
ENST00000408903.6:c.171-2512_171-2511delinsTA ENSP00000386227.3:n.171-2512_171-2511delinsTA
NM_001085377.1:c.171-2512_171-2511delinsTA NP_001078846.1:n.171-2512_171-2511delinsTA
XM_017009473.1:c.171-2512_171-2511delinsTA XP_016864962.1:n.171-2512_171-2511delinsTA
NM_001085377.2:c.171-2512_171-2511delinsTA MANE Select NP_001078846.2:n.171-2512_171-2511delinsTA