Canonical Allele Identifier: CA2638210890

Gene: GRN

Linked Data

• gnomAD v4: 17-44352324-G-GCAGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352325_44352326insAGACC , CM000679.2:g.44352325_44352326insAGACC	GRCh38
NC_000017.10:g.42429693_42429694insAGACC , CM000679.1:g.42429693_42429694insAGACC	GRCh37
NC_000017.9:g.39785219_39785220insAGACC	NCBI36
NG_007886.1:g.12203_12204insAGACC , LRG_661:g.12203_12204insAGACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-16_1414-15insAGACC MANE Select	ENSP00000053867.2:n.1414-16_1414-15insAGACC
ENST00000639447.1:c.1137-204_1137-203insAGACC	ENSP00000492014.1:n.1137-204_1137-203insAGACC
ENST00000053867.7:c.1414-16_1414-15insAGACC	ENSP00000053867.2:n.1414-16_1414-15insAGACC
ENST00000586242.1:c.48-16_48-15insAGACC
ENST00000586443.1:c.855-16_855-15insAGACC
ENST00000589265.5:c.943-16_943-15insAGACC	ENSP00000467616.1:n.943-16_943-15insAGACC
NM_002087.3:c.1414-16_1414-15insAGACC	NP_002078.1:n.1414-16_1414-15insAGACC
XM_005257253.1:c.1414-16_1414-15insAGACC	XP_005257310.1:n.1414-16_1414-15insAGACC
XM_024450730.1:c.1414-16_1414-15insAGACC	XP_024306498.1:n.1414-16_1414-15insAGACC
NM_002087.4:c.1414-16_1414-15insAGACC MANE Select	NP_002078.1:n.1414-16_1414-15insAGACC