Canonical Allele Identifier: CA2638209135

Gene: GRN

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351000C>A , CM000679.2:g.44351000C>A	GRCh38
NC_000017.10:g.42428368C>A , CM000679.1:g.42428368C>A	GRCh37
NC_000017.9:g.39783894C>A	NCBI36
NG_007886.1:g.10878C>A , LRG_661:g.10878C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.709-37C>A MANE Select	ENSP00000053867.2:n.709-37C>A
ENST00000639447.1:c.709-37C>A	ENSP00000492014.1:n.709-37C>A
ENST00000053867.7:c.709-37C>A	ENSP00000053867.2:n.709-37C>A
ENST00000585348.1:n.90C>A
ENST00000586443.1:c.150-37C>A
ENST00000586782.5:c.*119-37C>A	ENSP00000468318.1:n.*119-37C>A
ENST00000588237.5:c.511-37C>A	ENSP00000466611.1:n.511-37C>A
ENST00000589265.5:c.463-550C>A	ENSP00000467616.1:n.463-550C>A
ENST00000589923.1:n.30-37C>A
ENST00000590984.1:n.299-37C>A
NM_002087.3:c.709-37C>A	NP_002078.1:n.709-37C>A
XM_005257253.1:c.709-37C>A	XP_005257310.1:n.709-37C>A
XM_024450730.1:c.709-37C>A	XP_024306498.1:n.709-37C>A
NM_002087.4:c.709-37C>A MANE Select	NP_002078.1:n.709-37C>A