Canonical Allele Identifier: CA8601958

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350718C>T , CM000679.2:g.44350718C>T	GRCh38
NC_000017.10:g.42428086C>T , CM000679.1:g.42428086C>T	GRCh37
NC_000017.9:g.39783612C>T	NCBI36
NG_007886.1:g.10596C>T , LRG_661:g.10596C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.626C>T MANE Select	NP_002078.1:p.Pro209Leu
ENST00000053867.8:c.626C>T MANE Select	ENSP00000053867.2:p.Pro209Leu
NM_002087.3:c.626C>T	NP_002078.1:p.Pro209Leu
ENST00000053867.7:c.626C>T	ENSP00000053867.2:p.Pro209Leu
ENST00000586443.1:c.67C>T
ENST00000586782.5:c.*36C>T	ENSP00000468318.1:n.*36C>T
ENST00000588237.5:c.428C>T	ENSP00000466611.1:p.Pro143Leu
ENST00000589265.5:c.462+378C>T	ENSP00000467616.1:n.462+378C>T
ENST00000590984.1:n.216C>T
ENST00000639447.1:c.626C>T	ENSP00000492014.1:p.Pro209Leu
XM_005257253.1:c.626C>T	XP_005257310.1:p.Pro209Leu
XM_024450730.1:c.626C>T	XP_024306498.1:p.Pro209Leu