Canonical Allele Identifier: CA399764513

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42428166A>T (hg19) ; chr17:g.44350798A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350798A>T , CM000679.2:g.44350798A>T	GRCh38
NC_000017.10:g.42428166A>T , CM000679.1:g.42428166A>T	GRCh37
NC_000017.9:g.39783692A>T	NCBI36
NG_007886.1:g.10676A>T , LRG_661:g.10676A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000053867.8:c.706A>T MANE Select	ENSP00000053867.2:p.Asn236Tyr
ENST00000639447.1:c.706A>T	ENSP00000492014.1:p.Asn236Tyr
ENST00000053867.7:c.706A>T	ENSP00000053867.2:p.Asn236Tyr
ENST00000586443.1:c.147A>T
ENST00000586782.5:c.*116A>T	ENSP00000468318.1:n.*116A>T
ENST00000588237.5:c.508A>T	ENSP00000466611.1:p.Asn170Tyr
ENST00000589265.5:c.462+458A>T	ENSP00000467616.1:n.462+458A>T
ENST00000589923.1:n.27A>T
ENST00000590984.1:n.296A>T
NM_002087.3:c.706A>T	NP_002078.1:p.Asn236Tyr
XM_005257253.1:c.706A>T	XP_005257310.1:p.Asn236Tyr
XM_024450730.1:c.706A>T	XP_024306498.1:p.Asn236Tyr
NM_002087.4:c.706A>T MANE Select	NP_002078.1:p.Asn236Tyr