Canonical Allele Identifier: CA290925944

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350806_44350809del , CM000679.2:g.44350806_44350809del	GRCh38
NC_000017.10:g.42428174_42428177del , CM000679.1:g.42428174_42428177del	GRCh37
NC_000017.9:g.39783700_39783703del	NCBI36
NG_007886.1:g.10684_10687del , LRG_661:g.10684_10687del

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.708+6_708+9del MANE Select	NP_002078.1:n.708+6_708+9del
ENST00000053867.8:c.708+6_708+9del MANE Select	ENSP00000053867.2:n.708+6_708+9del
NM_002087.3:c.708+6_708+9del	NP_002078.1:n.708+6_708+9del
ENST00000053867.7:c.708+6_708+9del	ENSP00000053867.2:n.708+6_708+9del
ENST00000586443.1:c.149+6_149+9del
ENST00000586782.5:c.*118+6_*118+9del	ENSP00000468318.1:n.*118+6_*118+9del
ENST00000588237.5:c.510+6_510+9del	ENSP00000466611.1:n.510+6_510+9del
ENST00000589265.5:c.462+466_462+469del	ENSP00000467616.1:n.462+466_462+469del
ENST00000589923.1:n.29+6_29+9del
ENST00000590984.1:n.298+6_298+9del
ENST00000639447.1:c.708+6_708+9del	ENSP00000492014.1:n.708+6_708+9del
XM_005257253.1:c.708+6_708+9del	XP_005257310.1:n.708+6_708+9del
XM_024450730.1:c.708+6_708+9del	XP_024306498.1:n.708+6_708+9del