Canonical Allele Identifier: CA225191

Gene: GRN

Linked Data

• ClinVar Variation Id: 98118
• ClinVar RCV Id: RCV000084417
• dbSNP Id: rs63751020
• MyVariant Identifiers: chr17:g.42422705A>T (hg19) ; chr17:g.44345337A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44345337A>T , CM000679.2:g.44345337A>T	GRCh38
NC_000017.10:g.42422705A>T , CM000679.1:g.42422705A>T	GRCh37
NC_000017.9:g.39778231A>T	NCBI36
NG_007886.1:g.5215A>T , LRG_661:g.5215A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.-8+3A>T MANE Select	ENSP00000053867.2:n.-8+3A>T
ENST00000053867.7:c.-8+3A>T	ENSP00000053867.2:n.-8+3A>T
ENST00000585512.5:c.-416A>T	ENSP00000467745.1:n.-416A>T
ENST00000586782.5:c.-8+3A>T	ENSP00000468318.1:n.-8+3A>T
ENST00000587109.5:c.-276A>T	ENSP00000466271.1:n.-276A>T
ENST00000587387.5:c.-8+3A>T	ENSP00000467431.1:n.-8+3A>T
ENST00000587518.5:c.-48+3A>T	ENSP00000465518.1:n.-48+3A>T
ENST00000587958.1:n.29+3A>T
ENST00000588143.5:c.-4+3A>T	ENSP00000465375.1:n.-4+3A>T
ENST00000588170.5:n.89+3A>T
ENST00000588237.5:c.-8+3A>T	ENSP00000466611.1:n.-8+3A>T
ENST00000589265.5:c.-8+3A>T	ENSP00000467616.1:n.-8+3A>T
ENST00000589536.5:c.-140+3A>T	ENSP00000466956.1:n.-140+3A>T
ENST00000591740.5:c.-148+3A>T	ENSP00000467022.1:n.-148+3A>T
ENST00000592323.5:n.33+3A>T
ENST00000592783.5:c.-83+3A>T	ENSP00000467870.1:n.-83+3A>T
ENST00000593167.5:c.-280+3A>T	ENSP00000466405.1:n.-280+3A>T
NM_002087.3:c.-8+3A>T	NP_002078.1:n.-8+3A>T
XM_005257253.1:c.-276A>T	XP_005257310.1:n.-276A>T
NM_002087.4:c.-8+3A>T MANE Select	NP_002078.1:n.-8+3A>T