Canonical Allele Identifier: CA15835187
Gene: GREM1 HGNC NCBI

Linked Data

dbSNP Id: rs10318

Genomic Alleles

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

Transcript Alleles

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