Canonical Allele Identifier: CA1556800622
Gene: CRHBP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.76968582_76968586delinsCAACT , CM000667.2:g.76968582_76968586delinsCAACT GRCh38
NC_000005.9:g.76264407_76264411delinsCAACT , CM000667.1:g.76264407_76264411delinsCAACT GRCh37
NC_000005.8:g.76300163_76300167delinsCAACT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000274368.9:c.812-146_812-142delinsCAACT MANE Select ENSP00000274368.4:n.812-146_812-142delins...
ENST00000274368.8:c.812-146_812-142delinsCAACT ENSP00000274368.4:n.812-146_812-142delins...
ENST00000503763.1:n.227-146_227-142delinsCAACT
ENST00000514258.1:n.311+5122_311+5126delinsCAACT
NM_001882.3:c.812-146_812-142delinsCAACT NP_001873.2:n.812-146_812-142delinsCAACT
XR_948235.1:n.1111+5122_1111+5126delinsCAACT
XR_948235.3:n.1091+5122_1091+5126delinsCAACT
NM_001882.4:c.812-146_812-142delinsCAACT MANE Select NP_001873.2:n.812-146_812-142delinsCAACT