Canonical Allele Identifier: CA399766600

Gene: GRN

Linked Data

• MyVariant Identifiers: chr17:g.42429156T>C (hg19) ; chr17:g.44351788T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44351788T>C , CM000679.2:g.44351788T>C	GRCh38
NC_000017.10:g.42429156T>C , CM000679.1:g.42429156T>C	GRCh37
NC_000017.9:g.39784682T>C	NCBI36
NG_007886.1:g.11666T>C , LRG_661:g.11666T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000053867.8:c.1172T>C MANE Select	ENSP00000053867.2:p.Ile391Thr
ENST00000639447.1:c.1136+36T>C	ENSP00000492014.1:n.1136+36T>C
ENST00000053867.7:c.1172T>C	ENSP00000053867.2:p.Ile391Thr
ENST00000586443.1:c.613T>C
ENST00000589265.5:c.701T>C	ENSP00000467616.1:p.Ile234Thr
ENST00000589923.1:n.430T>C
NM_002087.3:c.1172T>C	NP_002078.1:p.Ile391Thr
XM_005257253.1:c.1172T>C	XP_005257310.1:p.Ile391Thr
XM_024450730.1:c.1172T>C	XP_024306498.1:p.Ile391Thr
NM_002087.4:c.1172T>C MANE Select	NP_002078.1:p.Ile391Thr