Canonical Allele Identifier: CA290926951

Gene: GRN

Linked Data

• ClinVar Variation Id: 2419137
• ClinVar RCV Id: RCV003112381
• dbSNP Id: rs63751698

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352326_44352518del , CM000679.2:g.44352326_44352518del	GRCh38
NC_000017.10:g.42429694_42429886del , CM000679.1:g.42429694_42429886del	GRCh37
NC_000017.9:g.39785220_39785412del	NCBI36
NG_007886.1:g.12204_12396del , LRG_661:g.12204_12396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-15_1591del
ENST00000639447.1:c.1137-203_1137-11del	ENSP00000492014.1:n.1137-203_1137-11del
ENST00000053867.7:c.1414-15_1591del
ENST00000586242.1:c.48-15_225del
ENST00000586443.1:c.855-15_1032del
ENST00000589265.5:c.943-15_1120del
NM_002087.3:c.1414-15_1591del
XM_005257253.1:c.1414-15_1591del
XM_024450730.1:c.1414-15_1591del
NM_002087.4:c.1414-15_1591del