Canonical Allele Identifier: CA8602016

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351131C>T , CM000679.2:g.44351131C>T	GRCh38
NC_000017.10:g.42428499C>T , CM000679.1:g.42428499C>T	GRCh37
NC_000017.9:g.39784025C>T	NCBI36
NG_007886.1:g.11009C>T , LRG_661:g.11009C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.803C>T MANE Select	NP_002078.1:p.Thr268Met
ENST00000053867.8:c.803C>T MANE Select	ENSP00000053867.2:p.Thr268Met
NM_002087.3:c.803C>T	NP_002078.1:p.Thr268Met
ENST00000053867.7:c.803C>T	ENSP00000053867.2:p.Thr268Met
ENST00000585348.1:n.221C>T
ENST00000586443.1:c.244C>T
ENST00000586782.5:c.*213C>T	ENSP00000468318.1:n.*213C>T
ENST00000589265.5:c.463-419C>T	ENSP00000467616.1:n.463-419C>T
ENST00000589923.1:n.93+31C>T
ENST00000590984.1:n.393C>T
ENST00000639447.1:c.803C>T	ENSP00000492014.1:p.Thr268Met
XM_005257253.1:c.803C>T	XP_005257310.1:p.Thr268Met
XM_024450730.1:c.803C>T	XP_024306498.1:p.Thr268Met