Canonical Allele Identifier: CA772280790

Gene: GRN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44346188C>A , CM000679.2:g.44346188C>A	GRCh38
NC_000017.10:g.42423556C>A , CM000679.1:g.42423556C>A	GRCh37
NC_000017.9:g.39779082C>A	NCBI36
NG_007886.1:g.6066C>A , LRG_661:g.6066C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.-8+854C>A MANE Select	ENSP00000053867.2:n.-8+854C>A
ENST00000053867.7:c.-8+854C>A	ENSP00000053867.2:n.-8+854C>A
ENST00000585512.5:c.-48C>A	ENSP00000467745.1:n.-48C>A
ENST00000586782.5:c.-8+854C>A	ENSP00000468318.1:n.-8+854C>A
ENST00000587109.5:c.-8+583C>A	ENSP00000466271.1:n.-8+583C>A
ENST00000587387.5:c.-8+854C>A	ENSP00000467431.1:n.-8+854C>A
ENST00000587518.5:c.-8+583C>A	ENSP00000465518.1:n.-8+583C>A
ENST00000587958.1:n.29+854C>A
ENST00000588143.5:c.-4+854C>A	ENSP00000465375.1:n.-4+854C>A
ENST00000588170.5:n.89+854C>A
ENST00000588237.5:c.-8+854C>A	ENSP00000466611.1:n.-8+854C>A
ENST00000589265.5:c.-8+854C>A	ENSP00000467616.1:n.-8+854C>A
ENST00000589536.5:c.-8+447C>A	ENSP00000466956.1:n.-8+447C>A
ENST00000591740.5:c.-48C>A	ENSP00000467022.1:n.-48C>A
ENST00000592323.5:n.33+854C>A
ENST00000592783.5:c.-8+583C>A	ENSP00000467870.1:n.-8+583C>A
ENST00000593167.5:c.-48C>A	ENSP00000466405.1:n.-48C>A
NM_002087.3:c.-8+854C>A	NP_002078.1:n.-8+854C>A
XM_005257253.1:c.-8+583C>A	XP_005257310.1:n.-8+583C>A
XM_024450730.1:c.-8+447C>A	XP_024306498.1:n.-8+447C>A
NM_002087.4:c.-8+854C>A MANE Select	NP_002078.1:n.-8+854C>A