Canonical Allele Identifier: CA2261354609

Gene: GRN

Linked Data

• dbSNP Id: rs2048384668

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352325_44352329del , CM000679.2:g.44352325_44352329del	GRCh38
NC_000017.10:g.42429693_42429697del , CM000679.1:g.42429693_42429697del	GRCh37
NC_000017.9:g.39785219_39785223del	NCBI36
NG_007886.1:g.12203_12207del , LRG_661:g.12203_12207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-16_1414-12del MANE Select	ENSP00000053867.2:n.1414-16_1414-12del
ENST00000639447.1:c.1137-204_1137-200del	ENSP00000492014.1:n.1137-204_1137-200del
ENST00000053867.7:c.1414-16_1414-12del	ENSP00000053867.2:n.1414-16_1414-12del
ENST00000586242.1:c.48-16_48-12del
ENST00000586443.1:c.855-16_855-12del
ENST00000589265.5:c.943-16_943-12del	ENSP00000467616.1:n.943-16_943-12del
NM_002087.3:c.1414-16_1414-12del	NP_002078.1:n.1414-16_1414-12del
XM_005257253.1:c.1414-16_1414-12del	XP_005257310.1:n.1414-16_1414-12del
XM_024450730.1:c.1414-16_1414-12del	XP_024306498.1:n.1414-16_1414-12del
NM_002087.4:c.1414-16_1414-12del MANE Select	NP_002078.1:n.1414-16_1414-12del