Canonical Allele Identifier: CA2168472760
Gene: GREM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.32734466A= , CM000677.2:g.32734466A= GRCh38
NC_000015.9:g.33026667A= , CM000677.1:g.33026667A= GRCh37
NC_000015.8:g.30813959A= NCBI36
NG_033791.1:g.21463A=
NG_033791.2:g.21463A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651154.1:c.*3221A= MANE Select ENSP00000498748.1:n.*3221A=
ENST00000652365.1:c.*3221A= ENSP00000498763.1:n.*3221A=
ENST00000622074.1:c.*3221A= ENSP00000478319.1:n.*3221A=
NM_001191322.1:c.*3221A= NP_001178251.1:n.*3221A=
NM_001191323.1:c.*3221A= NP_001178252.1:n.*3221A=
NM_013372.6:c.*3221A= NP_037504.1:n.*3221A=
XM_005254301.1:c.*3221A= XP_005254358.1:n.*3221A=
XM_017022077.1:c.*3221A= XP_016877566.1:n.*3221A=
NM_013372.7:c.*3221A= MANE Select NP_037504.1:n.*3221A=
NM_001191322.2:c.*3221A= NP_001178251.1:n.*3221A=
NM_001191323.2:c.*3221A= NP_001178252.1:n.*3221A=
NM_001368719.1:c.*3221A= NP_001355648.1:n.*3221A=