Canonical Allele Identifier: CA764687413

Gene: MREG PECR

Linked Data

• dbSNP Id: rs1358062491
• MyVariant Identifiers: chr2:g.216898718_216898719insC (hg19) ; chr2:g.216033995_216033996insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216033995_216033996insC , CM000664.2:g.216033995_216033996insC	GRCh38
NC_000002.11:g.216898718_216898719insC , CM000664.1:g.216898718_216898719insC	GRCh37
NC_000002.10:g.216606963_216606964insC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000424992.5:c.-102_-101insG (MREG)	ENSP00000413302.1:n.-102_-101insG
ENST00000442122.5:c.*440+5195_*440+5196insG (PECR)	ENSP00000395512.1:n.*440+5195_*440+5196insG
XR_001738847.2:n.1056-1144_1056-1143insG (PECR)
NM_001372189.1:c.-102_-101insG (MREG)	NP_001359118.1:n.-102_-101insG