Canonical Allele Identifier: CA399764541

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42428412G>A (hg19) ; chr17:g.44351044G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351044G>A , CM000679.2:g.44351044G>A	GRCh38
NC_000017.10:g.42428412G>A , CM000679.1:g.42428412G>A	GRCh37
NC_000017.9:g.39783938G>A	NCBI36
NG_007886.1:g.10922G>A , LRG_661:g.10922G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.716G>A MANE Select	ENSP00000053867.2:p.Cys239Tyr
ENST00000639447.1:c.716G>A	ENSP00000492014.1:p.Cys239Tyr
ENST00000053867.7:c.716G>A	ENSP00000053867.2:p.Cys239Tyr
ENST00000585348.1:n.134G>A
ENST00000586443.1:c.157G>A
ENST00000586782.5:c.*126G>A	ENSP00000468318.1:n.*126G>A
ENST00000588237.5:c.518G>A
ENST00000589265.5:c.463-506G>A	ENSP00000467616.1:n.463-506G>A
ENST00000589923.1:n.37G>A
ENST00000590984.1:n.306G>A
NM_002087.3:c.716G>A	NP_002078.1:p.Cys239Tyr
XM_005257253.1:c.716G>A	XP_005257310.1:p.Cys239Tyr
XM_024450730.1:c.716G>A	XP_024306498.1:p.Cys239Tyr
NM_002087.4:c.716G>A MANE Select	NP_002078.1:p.Cys239Tyr