Canonical Allele Identifier: CA2638210726
Gene: GRN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44352250_44352341del , CM000679.2:g.44352250_44352341del GRCh38
NC_000017.10:g.42429618_42429709del , CM000679.1:g.42429618_42429709del GRCh37
NC_000017.9:g.39785144_39785235del NCBI36
NG_007886.1:g.12128_12219del , LRG_661:g.12128_12219del

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1413+2_1414del
ENST00000639447.1:c.1137-279_1137-188del ENSP00000492014.1:n.1137-279_1137-188del
ENST00000053867.7:c.1413+2_1414del
ENST00000586242.1:c.47+2_48del
ENST00000586443.1:c.854+2_855del
ENST00000589265.5:c.942+2_943del
NM_002087.3:c.1413+2_1414del
XM_005257253.1:c.1413+2_1414del
XM_024450730.1:c.1413+2_1414del
NM_002087.4:c.1413+2_1414del