Canonical Allele Identifier: CA1445844258
Gene: CCKAR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490068A= , CM000666.2:g.26490068A= GRCh38
NC_000004.11:g.26491690A= , CM000666.1:g.26491690A= GRCh37
NC_000004.10:g.26100788A= NCBI36
NG_012053.1:g.5353T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000295589.4:c.112+88T= MANE Select ENSP00000295589.3:n.112+88T=
ENST00000295589.3:c.112+88T= ENSP00000295589.3:n.112+88T=
NM_000730.2:c.112+88T= NP_000721.1:n.112+88T=
NM_000730.3:c.112+88T= MANE Select NP_000721.1:n.112+88T=