Canonical Allele Identifier: CA1445844277
Gene: CCKAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490117A= , CM000666.2:g.26490117A= GRCh38
NC_000004.11:g.26491739A= , CM000666.1:g.26491739A= GRCh37
NC_000004.10:g.26100837A= NCBI36
NG_012053.1:g.5304T=

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+39T= MANE Select ENSP00000295589.3:n.112+39T=
ENST00000295589.3:c.112+39T= ENSP00000295589.3:n.112+39T=
NM_000730.2:c.112+39T= NP_000721.1:n.112+39T=
NM_000730.3:c.112+39T= MANE Select NP_000721.1:n.112+39T=
Search 100 bp 5'
Search 100 bp 3'