Canonical Allele Identifier: CA399760283

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44349665A>T , CM000679.2:g.44349665A>T	GRCh38
NC_000017.10:g.42427033A>T , CM000679.1:g.42427033A>T	GRCh37
NC_000017.9:g.39782559A>T	NCBI36
NG_007886.1:g.9543A>T , LRG_661:g.9543A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.265-2A>T MANE Select	NP_002078.1:n.265-2A>T
ENST00000053867.8:c.265-2A>T MANE Select	ENSP00000053867.2:n.265-2A>T
NM_002087.3:c.265-2A>T	NP_002078.1:n.265-2A>T
ENST00000053867.7:c.265-2A>T	ENSP00000053867.2:n.265-2A>T
ENST00000586782.5:c.265-2A>T	ENSP00000468318.1:n.265-2A>T
ENST00000587387.5:c.305A>T	ENSP00000467431.1:p.Gln102Leu
ENST00000587518.5:c.265-2A>T	ENSP00000465518.1:n.265-2A>T
ENST00000587958.1:n.414A>T
ENST00000588143.5:c.265-2A>T	ENSP00000465375.1:n.265-2A>T
ENST00000588170.5:n.361-2A>T
ENST00000588237.5:c.264+114A>T	ENSP00000466611.1:n.264+114A>T
ENST00000589265.5:c.265-2A>T	ENSP00000467616.1:n.265-2A>T
ENST00000589536.5:c.265-2A>T	ENSP00000466956.1:n.265-2A>T
ENST00000591740.5:c.265-2A>T	ENSP00000467022.1:n.265-2A>T
ENST00000592323.5:n.428-2A>T
ENST00000592783.5:c.265-2A>T	ENSP00000467870.1:n.265-2A>T
ENST00000593167.5:c.265-2A>T	ENSP00000466405.1:n.265-2A>T
ENST00000639447.1:c.265-2A>T	ENSP00000492014.1:n.265-2A>T
XM_005257253.1:c.265-2A>T	XP_005257310.1:n.265-2A>T
XM_024450730.1:c.265-2A>T	XP_024306498.1:n.265-2A>T