Canonical Allele Identifier: CA2261354299

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351732_44351742delinsTCCCTCCTCCG , CM000679.2:g.44351732_44351742delinsTCCCTCCTCCG	GRCh38
NC_000017.10:g.42429100_42429110delinsTCCCTCCTCCG , CM000679.1:g.42429100_42429110delinsTCCCTCCTCCG	GRCh37
NC_000017.9:g.39784626_39784636delinsTCCCTCCTCCG	NCBI36
NG_007886.1:g.11610_11620delinsTCCCTCCTCCG , LRG_661:g.11610_11620delinsTCCCTCCTCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1116_1126delinsTCCCTCCTCCG MANE Select	ENSP00000053867.2:p.Cys372=
ENST00000639447.1:c.1116_1126delinsTCCCTCCTCCG	ENSP00000492014.1:p.Cys372=
ENST00000053867.7:c.1116_1126delinsTCCCTCCTCCG	ENSP00000053867.2:p.Cys372=
ENST00000586443.1:c.557_567delinsTCCCTCCTCCG
ENST00000589265.5:c.645_655delinsTCCCTCCTCCG	ENSP00000467616.1:p.Cys215=
ENST00000589923.1:n.374_384delinsTCCCTCCTCCG
NM_002087.3:c.1116_1126delinsTCCCTCCTCCG	NP_002078.1:p.Cys372=
XM_005257253.1:c.1116_1126delinsTCCCTCCTCCG	XP_005257310.1:p.Cys372=
XM_024450730.1:c.1116_1126delinsTCCCTCCTCCG	XP_024306498.1:p.Cys372=
NM_002087.4:c.1116_1126delinsTCCCTCCTCCG MANE Select	NP_002078.1:p.Cys372=