Canonical Allele Identifier: CA93702523
Gene: CCKAR HGNC NCBI

Linked Data

dbSNP Id: rs762243830

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.26490138_26490140del , CM000666.2:g.26490138_26490140del GRCh38
NC_000004.11:g.26491760_26491762del , CM000666.1:g.26491760_26491762del GRCh37
NC_000004.10:g.26100858_26100860del NCBI36
NG_012053.1:g.5282_5284del

Transcript Alleles

HGVS Amino-acid change
ENST00000295589.4:c.112+17_112+19del MANE Select ENSP00000295589.3:n.112+17_112+19del
ENST00000295589.3:c.112+17_112+19del ENSP00000295589.3:n.112+17_112+19del
NM_000730.2:c.112+17_112+19del NP_000721.1:n.112+17_112+19del
NM_000730.3:c.112+17_112+19del MANE Select NP_000721.1:n.112+17_112+19del