Canonical Allele Identifier: CA1445844281
Gene: CCKAR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490131T= , CM000666.2:g.26490131T= GRCh38
NC_000004.11:g.26491753T= , CM000666.1:g.26491753T= GRCh37
NC_000004.10:g.26100851T= NCBI36
NG_012053.1:g.5290A=

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+25A= MANE Select ENSP00000295589.3:n.112+25A=
ENST00000295589.3:c.112+25A= ENSP00000295589.3:n.112+25A=
NM_000730.2:c.112+25A= NP_000721.1:n.112+25A=
NM_000730.3:c.112+25A= MANE Select NP_000721.1:n.112+25A=
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