Canonical Allele Identifier: CA8601967

Gene: GRN

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44350754G>C , CM000679.2:g.44350754G>C	GRCh38
NC_000017.10:g.42428122G>C , CM000679.1:g.42428122G>C	GRCh37
NC_000017.9:g.39783648G>C	NCBI36
NG_007886.1:g.10632G>C , LRG_661:g.10632G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002087.4:c.662G>C MANE Select	NP_002078.1:p.Cys221Ser
ENST00000053867.8:c.662G>C MANE Select	ENSP00000053867.2:p.Cys221Ser
NM_002087.3:c.662G>C	NP_002078.1:p.Cys221Ser
ENST00000053867.7:c.662G>C	ENSP00000053867.2:p.Cys221Ser
ENST00000586443.1:c.103G>C
ENST00000586782.5:c.*72G>C	ENSP00000468318.1:n.*72G>C
ENST00000588237.5:c.464G>C	ENSP00000466611.1:p.Cys155Ser
ENST00000589265.5:c.462+414G>C	ENSP00000467616.1:n.462+414G>C
ENST00000590984.1:n.252G>C
ENST00000639447.1:c.662G>C	ENSP00000492014.1:p.Cys221Ser
XM_005257253.1:c.662G>C	XP_005257310.1:p.Cys221Ser
XM_024450730.1:c.662G>C	XP_024306498.1:p.Cys221Ser