Canonical Allele Identifier: CA2168506174

Gene: GREM1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32720301A>C , CM000677.2:g.32720301A>C	GRCh38
NC_000015.9:g.33012502A>C , CM000677.1:g.33012502A>C	GRCh37
NC_000015.8:g.30799794A>C	NCBI36
NG_033791.1:g.7298A>C
NG_033791.2:g.7298A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651154.1:c.-2+2140A>C MANE Select	ENSP00000498748.1:n.-2+2140A>C
ENST00000652365.1:c.-2+1599A>C	ENSP00000498763.1:n.-2+1599A>C
ENST00000560677.5:c.-2+2140A>C	ENSP00000453387.1:n.-2+2140A>C
ENST00000560830.1:c.-2+2140A>C	ENSP00000453141.1:n.-2+2140A>C
ENST00000622074.1:c.-2+2140A>C	ENSP00000478319.1:n.-2+2140A>C
NM_001191322.1:c.-2+2140A>C	NP_001178251.1:n.-2+2140A>C
NM_001191323.1:c.-2+2140A>C	NP_001178252.1:n.-2+2140A>C
NM_013372.6:c.-2+2140A>C	NP_037504.1:n.-2+2140A>C
XM_005254301.1:c.167+2140A>C	XP_005254358.1:n.167+2140A>C
XM_017022077.1:c.110+1599A>C	XP_016877566.1:n.110+1599A>C
NM_013372.7:c.-2+2140A>C MANE Select	NP_037504.1:n.-2+2140A>C
NM_001191322.2:c.-2+2140A>C	NP_001178251.1:n.-2+2140A>C
NM_001191323.2:c.-2+2140A>C	NP_001178252.1:n.-2+2140A>C
NM_001368719.1:c.-2+1599A>C	NP_001355648.1:n.-2+1599A>C