Canonical Allele Identifier: CA802099973

Gene: MCC

Linked Data

• dbSNP Id: rs1188132747
• MyVariant Identifiers: chr5:g.112723481_112723496del (hg19) ; chr5:g.113387784_113387799del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.113387790_113387805del , CM000667.2:g.113387790_113387805del	GRCh38
NC_000005.9:g.112723487_112723502del , CM000667.1:g.112723487_112723502del	GRCh37
NC_000005.8:g.112751386_112751401del	NCBI36
NG_012265.1:g.106032_106047del

Transcript Alleles

HGVS	Amino-acid change
ENST00000408903.7:c.171-2587_171-2572del MANE Select	ENSP00000386227.3:n.171-2587_171-2572del
ENST00000408903.6:c.171-2587_171-2572del	ENSP00000386227.3:n.171-2587_171-2572del
NM_001085377.1:c.171-2587_171-2572del	NP_001078846.1:n.171-2587_171-2572del
XM_017009473.1:c.171-2587_171-2572del	XP_016864962.1:n.171-2587_171-2572del
NM_001085377.2:c.171-2587_171-2572del MANE Select	NP_001078846.2:n.171-2587_171-2572del