Canonical Allele Identifier: CA1445844230
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs1737526857

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490006_26490008dup , CM000666.2:g.26490006_26490008dup GRCh38
NC_000004.11:g.26491628_26491630dup , CM000666.1:g.26491628_26491630dup GRCh37
NC_000004.10:g.26100726_26100728dup NCBI36
NG_012053.1:g.5413_5415dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000295589.4:c.112+148_112+150dup MANE Select ENSP00000295589.3:n.112+148_112+150dup
ENST00000295589.3:c.112+148_112+150dup ENSP00000295589.3:n.112+148_112+150dup
NM_000730.2:c.112+148_112+150dup NP_000721.1:n.112+148_112+150dup
NM_000730.3:c.112+148_112+150dup MANE Select NP_000721.1:n.112+148_112+150dup