Canonical Allele Identifier: CA2638209639

Gene: GRN

Linked Data

• gnomAD v4: 17-44351622-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351624dup , CM000679.2:g.44351624dup	GRCh38
NC_000017.10:g.42428992dup , CM000679.1:g.42428992dup	GRCh37
NC_000017.9:g.39784518dup	NCBI36
NG_007886.1:g.11502dup , LRG_661:g.11502dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1008dup MANE Select	ENSP00000053867.2:p.Gln337ThrfsTer?
ENST00000639447.1:c.1008dup	ENSP00000492014.1:p.Gln337ThrfsTer?
ENST00000053867.7:c.1008dup	ENSP00000053867.2:p.Gln337ThrfsTer?
ENST00000586443.1:c.449dup
ENST00000589265.5:c.537dup	ENSP00000467616.1:p.Gln180ThrfsTer?
ENST00000589923.1:n.266dup
NM_002087.3:c.1008dup	NP_002078.1:p.Gln337ThrfsTer?
XM_005257253.1:c.1008dup	XP_005257310.1:p.Gln337ThrfsTer?
XM_024450730.1:c.1008dup	XP_024306498.1:p.Gln337ThrfsTer?
NM_002087.4:c.1008dup MANE Select	NP_002078.1:p.Gln337ThrfsTer?