Canonical Allele Identifier: CA2261354550

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44352205_44352206delinsGC , CM000679.2:g.44352205_44352206delinsGC	GRCh38
NC_000017.10:g.42429573_42429574delinsGC , CM000679.1:g.42429573_42429574delinsGC	GRCh37
NC_000017.9:g.39785099_39785100delinsGC	NCBI36
NG_007886.1:g.12083_12084delinsGC , LRG_661:g.12083_12084delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1370_1371delinsGC MANE Select	ENSP00000053867.2:p.Cys457=
ENST00000639447.1:c.1137-324_1137-323delinsGC	ENSP00000492014.1:n.1137-324_1137-323delinsGC
ENST00000053867.7:c.1370_1371delinsGC	ENSP00000053867.2:p.Cys457=
ENST00000586242.1:c.4_5delinsGC
ENST00000586443.1:c.811_812delinsGC
ENST00000589265.5:c.899_900delinsGC	ENSP00000467616.1:p.Cys300=
NM_002087.3:c.1370_1371delinsGC	NP_002078.1:p.Cys457=
XM_005257253.1:c.1370_1371delinsGC	XP_005257310.1:p.Cys457=
XM_024450730.1:c.1370_1371delinsGC	XP_024306498.1:p.Cys457=
NM_002087.4:c.1370_1371delinsGC MANE Select	NP_002078.1:p.Cys457=