Canonical Allele Identifier: CA2261354314

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351755_44351758delinsAACT , CM000679.2:g.44351755_44351758delinsAACT	GRCh38
NC_000017.10:g.42429123_42429126delinsAACT , CM000679.1:g.42429123_42429126delinsAACT	GRCh37
NC_000017.9:g.39784649_39784652delinsAACT	NCBI36
NG_007886.1:g.11633_11636delinsAACT , LRG_661:g.11633_11636delinsAACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1139_1142delinsAACT MANE Select	ENSP00000053867.2:p.Gln380=
ENST00000639447.1:c.1136+3_1136+6delinsAACT	ENSP00000492014.1:n.1136+3_1136+6delinsAACT
ENST00000053867.7:c.1139_1142delinsAACT	ENSP00000053867.2:p.Gln380=
ENST00000586443.1:c.580_583delinsAACT
ENST00000589265.5:c.668_671delinsAACT	ENSP00000467616.1:p.Gln223=
ENST00000589923.1:n.397_400delinsAACT
NM_002087.3:c.1139_1142delinsAACT	NP_002078.1:p.Gln380=
XM_005257253.1:c.1139_1142delinsAACT	XP_005257310.1:p.Gln380=
XM_024450730.1:c.1139_1142delinsAACT	XP_024306498.1:p.Gln380=
NM_002087.4:c.1139_1142delinsAACT MANE Select	NP_002078.1:p.Gln380=