Canonical Allele Identifier: CA2261354479

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352061_44352063delinsCGT , CM000679.2:g.44352061_44352063delinsCGT	GRCh38
NC_000017.10:g.42429429_42429431delinsCGT , CM000679.1:g.42429429_42429431delinsCGT	GRCh37
NC_000017.9:g.39784955_39784957delinsCGT	NCBI36
NG_007886.1:g.11939_11941delinsCGT , LRG_661:g.11939_11941delinsCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1226_1228delinsCGT MANE Select	ENSP00000053867.2:p.Thr409=
ENST00000639447.1:c.1136+309_1136+311delinsCGT	ENSP00000492014.1:n.1136+309_1136+311delinsCGT
ENST00000053867.7:c.1226_1228delinsCGT	ENSP00000053867.2:p.Thr409=
ENST00000586443.1:c.667_669delinsCGT
ENST00000589265.5:c.755_757delinsCGT	ENSP00000467616.1:p.Thr252=
NM_002087.3:c.1226_1228delinsCGT	NP_002078.1:p.Thr409=
XM_005257253.1:c.1226_1228delinsCGT	XP_005257310.1:p.Thr409=
XM_024450730.1:c.1226_1228delinsCGT	XP_024306498.1:p.Thr409=
NM_002087.4:c.1226_1228delinsCGT MANE Select	NP_002078.1:p.Thr409=