Canonical Allele Identifier: CA2695226230

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351628_44351629delinsC , CM000679.2:g.44351628_44351629delinsC	GRCh38
NC_000017.10:g.42428996_42428997delinsC , CM000679.1:g.42428996_42428997delinsC	GRCh37
NC_000017.9:g.39784522_39784523delinsC	NCBI36
NG_007886.1:g.11506_11507delinsC , LRG_661:g.11506_11507delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1012_1013delinsC MANE Select	ENSP00000053867.2:p.Gly338ArgfsTer23
ENST00000639447.1:c.1012_1013delinsC	ENSP00000492014.1:p.Gly338ArgfsTer23
ENST00000053867.7:c.1012_1013delinsC	ENSP00000053867.2:p.Gly338ArgfsTer23
ENST00000586443.1:c.453_454delinsC
ENST00000589265.5:c.541_542delinsC	ENSP00000467616.1:p.Gly181ArgfsTer23
ENST00000589923.1:n.270_271delinsC
NM_002087.3:c.1012_1013delinsC	NP_002078.1:p.Gly338ArgfsTer23
XM_005257253.1:c.1012_1013delinsC	XP_005257310.1:p.Gly338ArgfsTer23
XM_024450730.1:c.1012_1013delinsC	XP_024306498.1:p.Gly338ArgfsTer23
NM_002087.4:c.1012_1013delinsC MANE Select	NP_002078.1:p.Gly338ArgfsTer23