Canonical Allele Identifier: CA2578103154
Gene: CCKAR HGNC NCBI

Linked Data

gnomAD v4: 4-26490146-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490146C>A , CM000666.2:g.26490146C>A GRCh38
NC_000004.11:g.26491768C>A , CM000666.1:g.26491768C>A GRCh37
NC_000004.10:g.26100866C>A NCBI36
NG_012053.1:g.5275G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+10G>T MANE Select ENSP00000295589.3:n.112+10G>T
ENST00000295589.3:c.112+10G>T ENSP00000295589.3:n.112+10G>T
NM_000730.2:c.112+10G>T NP_000721.1:n.112+10G>T
NM_000730.3:c.112+10G>T MANE Select NP_000721.1:n.112+10G>T