Canonical Allele Identifier: CA561926343
Gene: MCC HGNC NCBI

Linked Data

dbSNP Id: rs1212507620
gnomAD v2: 5-112723728-C-CAT
gnomAD v3: 5-113388031-C-CAT
gnomAD v4: 5-113388031-C-CAT
MyVariant Identifiers: chr5:g.112723728_112723729insAT (hg19) chr5:g.113388031_113388032insAT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113388036_113388037dup , CM000667.2:g.113388036_113388037dup GRCh38
NC_000005.9:g.112723733_112723734dup , CM000667.1:g.112723733_112723734dup GRCh37
NC_000005.8:g.112751632_112751633dup NCBI36
NG_012265.1:g.105798_105799dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000408903.7:c.171-2821_171-2820dup MANE Select ENSP00000386227.3:n.171-2821_171-2820dup
ENST00000408903.6:c.171-2821_171-2820dup ENSP00000386227.3:n.171-2821_171-2820dup
NM_001085377.1:c.171-2821_171-2820dup NP_001078846.1:n.171-2821_171-2820dup
XM_017009473.1:c.171-2821_171-2820dup XP_016864962.1:n.171-2821_171-2820dup
NM_001085377.2:c.171-2821_171-2820dup MANE Select NP_001078846.2:n.171-2821_171-2820dup
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