Canonical Allele Identifier: CA399764562

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42428421A>T (hg19) ; chr17:g.44351053A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351053A>T , CM000679.2:g.44351053A>T	GRCh38
NC_000017.10:g.42428421A>T , CM000679.1:g.42428421A>T	GRCh37
NC_000017.9:g.39783947A>T	NCBI36
NG_007886.1:g.10931A>T , LRG_661:g.10931A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.725A>T MANE Select	ENSP00000053867.2:p.Asp242Val
ENST00000639447.1:c.725A>T	ENSP00000492014.1:p.Asp242Val
ENST00000053867.7:c.725A>T	ENSP00000053867.2:p.Asp242Val
ENST00000585348.1:n.143A>T
ENST00000586443.1:c.166A>T
ENST00000586782.5:c.*135A>T	ENSP00000468318.1:n.*135A>T
ENST00000589265.5:c.463-497A>T	ENSP00000467616.1:n.463-497A>T
ENST00000589923.1:n.46A>T
ENST00000590984.1:n.315A>T
NM_002087.3:c.725A>T	NP_002078.1:p.Asp242Val
XM_005257253.1:c.725A>T	XP_005257310.1:p.Asp242Val
XM_024450730.1:c.725A>T	XP_024306498.1:p.Asp242Val
NM_002087.4:c.725A>T MANE Select	NP_002078.1:p.Asp242Val