Canonical Allele Identifier: CA290920957

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44345384dup , CM000679.2:g.44345384dup	GRCh38
NC_000017.10:g.42422752dup , CM000679.1:g.42422752dup	GRCh37
NC_000017.9:g.39778278dup	NCBI36
NG_007886.1:g.5262dup , LRG_661:g.5262dup

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.-8+50dup MANE Select	NP_002078.1:n.-8+50dup
ENST00000053867.8:c.-8+50dup MANE Select	ENSP00000053867.2:n.-8+50dup
NM_002087.3:c.-8+50dup	NP_002078.1:n.-8+50dup
ENST00000053867.7:c.-8+50dup	ENSP00000053867.2:n.-8+50dup
ENST00000585512.5:c.-369dup	ENSP00000467745.1:n.-369dup
ENST00000586782.5:c.-8+50dup	ENSP00000468318.1:n.-8+50dup
ENST00000587109.5:c.-229dup	ENSP00000466271.1:n.-229dup
ENST00000587387.5:c.-8+50dup	ENSP00000467431.1:n.-8+50dup
ENST00000587518.5:c.-48+50dup	ENSP00000465518.1:n.-48+50dup
ENST00000587958.1:n.29+50dup
ENST00000588143.5:c.-4+50dup	ENSP00000465375.1:n.-4+50dup
ENST00000588170.5:n.89+50dup
ENST00000588237.5:c.-8+50dup	ENSP00000466611.1:n.-8+50dup
ENST00000589265.5:c.-8+50dup	ENSP00000467616.1:n.-8+50dup
ENST00000589536.5:c.-140+50dup	ENSP00000466956.1:n.-140+50dup
ENST00000591740.5:c.-148+50dup	ENSP00000467022.1:n.-148+50dup
ENST00000592323.5:n.33+50dup
ENST00000592783.5:c.-83+50dup	ENSP00000467870.1:n.-83+50dup
ENST00000593167.5:c.-280+50dup	ENSP00000466405.1:n.-280+50dup
XM_005257253.1:c.-229dup	XP_005257310.1:n.-229dup