Canonical Allele Identifier: CA919846762

Gene: GRN

Linked Data

• dbSNP Id: rs1567888344
• gnomAD v4: 17-44352300-GACAGGA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352304_44352309del , CM000679.2:g.44352304_44352309del	GRCh38
NC_000017.10:g.42429672_42429677del , CM000679.1:g.42429672_42429677del	GRCh37
NC_000017.9:g.39785198_39785203del	NCBI36
NG_007886.1:g.12182_12187del , LRG_661:g.12182_12187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1414-37_1414-32del MANE Select	ENSP00000053867.2:n.1414-37_1414-32del
ENST00000639447.1:c.1137-225_1137-220del	ENSP00000492014.1:n.1137-225_1137-220del
ENST00000053867.7:c.1414-37_1414-32del	ENSP00000053867.2:n.1414-37_1414-32del
ENST00000586242.1:c.48-37_48-32del
ENST00000586443.1:c.855-37_855-32del
ENST00000589265.5:c.943-37_943-32del	ENSP00000467616.1:n.943-37_943-32del
NM_002087.3:c.1414-37_1414-32del	NP_002078.1:n.1414-37_1414-32del
XM_005257253.1:c.1414-37_1414-32del	XP_005257310.1:n.1414-37_1414-32del
XM_024450730.1:c.1414-37_1414-32del	XP_024306498.1:n.1414-37_1414-32del
NM_002087.4:c.1414-37_1414-32del MANE Select	NP_002078.1:n.1414-37_1414-32del