Canonical Allele Identifier: CA2261354418
Gene: GRN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351951A= , CM000679.2:g.44351951A= GRCh38
NC_000017.10:g.42429319A= , CM000679.1:g.42429319A= GRCh37
NC_000017.9:g.39784845A= NCBI36
NG_007886.1:g.11829A= , LRG_661:g.11829A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1180-64A= MANE Select ENSP00000053867.2:n.1180-64A=
ENST00000639447.1:c.1136+199A= ENSP00000492014.1:n.1136+199A=
ENST00000053867.7:c.1180-64A= ENSP00000053867.2:n.1180-64A=
ENST00000586443.1:c.621-64A=
ENST00000589265.5:c.709-64A= ENSP00000467616.1:n.709-64A=
NM_002087.3:c.1180-64A= NP_002078.1:n.1180-64A=
XM_005257253.1:c.1180-64A= XP_005257310.1:n.1180-64A=
XM_024450730.1:c.1180-64A= XP_024306498.1:n.1180-64A=
NM_002087.4:c.1180-64A= MANE Select NP_002078.1:n.1180-64A=