Canonical Allele Identifier: CA2172180600
Gene: CHP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41271720A= , CM000677.2:g.41271720A= GRCh38
NC_000015.9:g.41563918A= , CM000677.1:g.41563918A= GRCh37
NC_000015.8:g.39351210A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000334660.10:c.411+1102A= MANE Select ENSP00000335632.5:n.411+1102A=
ENST00000334660.9:c.411+1102A= ENSP00000335632.5:n.411+1102A=
ENST00000392151.6:c.350-7047A= ENSP00000440490.1:n.350-7047A=
ENST00000558351.5:n.543+1102A=
ENST00000560397.5:c.411+1102A= ENSP00000454007.1:n.411+1102A=
ENST00000560411.5:c.*176+1102A= ENSP00000453375.1:n.*176+1102A=
ENST00000560633.1:n.399-460A=
ENST00000560784.5:c.*110+1102A= ENSP00000452772.1:n.*110+1102A=
ENST00000560965.1:c.272-460A=
NM_007236.4:c.411+1102A= NP_009167.1:n.411+1102A=
NM_007236.5:c.411+1102A= MANE Select NP_009167.1:n.411+1102A=