Canonical Allele Identifier: CA1573788988
Gene: MCC HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113387854T= , CM000667.2:g.113387854T= GRCh38
NC_000005.9:g.112723551T= , CM000667.1:g.112723551T= GRCh37
NC_000005.8:g.112751450T= NCBI36
NG_012265.1:g.105977A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2642A= MANE Select ENSP00000386227.3:n.171-2642A=
ENST00000408903.6:c.171-2642A= ENSP00000386227.3:n.171-2642A=
NM_001085377.1:c.171-2642A= NP_001078846.1:n.171-2642A=
XM_017009473.1:c.171-2642A= XP_016864962.1:n.171-2642A=
NM_001085377.2:c.171-2642A= MANE Select NP_001078846.2:n.171-2642A=
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