Canonical Allele Identifier: CA891843125

Gene: MEN1

Linked Data

• ClinVar Variation Id: 572762
• ClinVar RCV Id: RCV000694224
• MyVariant Identifiers: chr11:g.64570986_64572288del (hg19) ; chr11:g.64803514_64804816del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64803514_64804816del , CM000673.2:g.64803514_64804816del	GRCh38
NC_000011.9:g.64570986_64572288del , CM000673.1:g.64570986_64572288del	GRCh37
NC_000011.8:g.64327562_64328864del	NCBI36
NG_033040.1:g.3426_4728del

Transcript Alleles

HGVS	Amino-acid change
ENST00000315422.9:c.1351_*820del	ENSP00000323747.4:n.[c.1351_*820del;Val45...
ENST00000377313.6:c.1366_*820del	ENSP00000366530.1:n.[c.1366_*820del;Val45...
ENST00000377316.6:c.1186_*820del	ENSP00000366533.1:n.[c.1186_*820del;Val39...
XM_005274001.3:c.1351_*820del	XP_005274058.1:n.[c.1351_*820del;Val451=]...