Canonical Allele Identifier: CA2168472458

Gene: GREM1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.32733778C= , CM000677.2:g.32733778C=	GRCh38
NC_000015.9:g.33025979C= , CM000677.1:g.33025979C=	GRCh37
NC_000015.8:g.30813271C=	NCBI36
NG_033791.1:g.20775C=
NG_033791.2:g.20775C=

Transcript Alleles

HGVS	Amino-acid Change
NM_013372.7:c.*2533C= MANE Select	NP_037504.1:n.*2533C=
ENST00000651154.1:c.*2533C= MANE Select	ENSP00000498748.1:n.*2533C=
NM_001191322.1:c.*2533C=	NP_001178251.1:n.*2533C=
NM_001191322.2:c.*2533C=	NP_001178251.1:n.*2533C=
NM_001191323.1:c.*2533C=	NP_001178252.1:n.*2533C=
NM_001191323.2:c.*2533C=	NP_001178252.1:n.*2533C=
NM_001368719.1:c.*2533C=	NP_001355648.1:n.*2533C=
NM_013372.6:c.*2533C=	NP_037504.1:n.*2533C=
ENST00000622074.1:c.*2533C=	ENSP00000478319.1:n.*2533C=
ENST00000652365.1:c.*2533C=	ENSP00000498763.1:n.*2533C=
XM_005254301.1:c.*2533C=	XP_005254358.1:n.*2533C=
XM_017022077.1:c.*2533C=	XP_016877566.1:n.*2533C=