Canonical Allele Identifier: CA399764322

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350753T>A , CM000679.2:g.44350753T>A	GRCh38
NC_000017.10:g.42428121T>A , CM000679.1:g.42428121T>A	GRCh37
NC_000017.9:g.39783647T>A	NCBI36
NG_007886.1:g.10631T>A , LRG_661:g.10631T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.661T>A MANE Select	NP_002078.1:p.Cys221Ser
ENST00000053867.8:c.661T>A MANE Select	ENSP00000053867.2:p.Cys221Ser
NM_002087.3:c.661T>A	NP_002078.1:p.Cys221Ser
ENST00000053867.7:c.661T>A	ENSP00000053867.2:p.Cys221Ser
ENST00000586443.1:c.102T>A
ENST00000586782.5:c.*71T>A	ENSP00000468318.1:n.*71T>A
ENST00000588237.5:c.463T>A	ENSP00000466611.1:p.Cys155Ser
ENST00000589265.5:c.462+413T>A	ENSP00000467616.1:n.462+413T>A
ENST00000590984.1:n.251T>A
ENST00000639447.1:c.661T>A	ENSP00000492014.1:p.Cys221Ser
XM_005257253.1:c.661T>A	XP_005257310.1:p.Cys221Ser
XM_024450730.1:c.661T>A	XP_024306498.1:p.Cys221Ser