Canonical Allele Identifier: CA2695226228

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351629_44351640del , CM000679.2:g.44351629_44351640del	GRCh38
NC_000017.10:g.42428997_42429008del , CM000679.1:g.42428997_42429008del	GRCh37
NC_000017.9:g.39784523_39784534del	NCBI36
NG_007886.1:g.11507_11518del , LRG_661:g.11507_11518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1013_1024del MANE Select	ENSP00000053867.2:p.Gly338_Gln341del
ENST00000639447.1:c.1013_1024del	ENSP00000492014.1:p.Gly338_Gln341del
ENST00000053867.7:c.1013_1024del	ENSP00000053867.2:p.Gly338_Gln341del
ENST00000586443.1:c.454_465del
ENST00000589265.5:c.542_553del	ENSP00000467616.1:p.Gly181_Gln184del
ENST00000589923.1:n.271_282del
NM_002087.3:c.1013_1024del	NP_002078.1:p.Gly338_Gln341del
XM_005257253.1:c.1013_1024del	XP_005257310.1:p.Gly338_Gln341del
XM_024450730.1:c.1013_1024del	XP_024306498.1:p.Gly338_Gln341del
NM_002087.4:c.1013_1024del MANE Select	NP_002078.1:p.Gly338_Gln341del