Canonical Allele Identifier: CA2061880873
Gene: CMKLR1 HGNC NCBI

Linked Data

dbSNP Id: rs1878022

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.108305255C>A , CM000674.2:g.108305255C>A GRCh38
NC_000012.11:g.108699032C>A , CM000674.1:g.108699032C>A GRCh37
NC_000012.10:g.107223162C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000550402.6:c.-73-11591G>T MANE Select ENSP00000449716.1:n.-73-11591G>T
ENST00000312143.11:c.-73-11591G>T ENSP00000311733.7:n.-73-11591G>T
ENST00000412676.5:c.-73-11591G>T ENSP00000401293.1:n.-73-11591G>T
ENST00000549466.1:c.-73-11591G>T ENSP00000448362.1:n.-73-11591G>T
ENST00000550402.5:c.-73-11591G>T ENSP00000449716.1:n.-73-11591G>T
ENST00000550573.5:c.-73-11591G>T ENSP00000448925.1:n.-73-11591G>T
ENST00000552995.5:c.-3-12296G>T ENSP00000447579.1:n.-3-12296G>T
NM_001142343.1:c.-73-11591G>T NP_001135815.1:n.-73-11591G>T
NM_001142344.1:c.-73-11591G>T NP_001135816.1:n.-73-11591G>T
NM_001142345.1:c.-73-11591G>T NP_001135817.1:n.-73-11591G>T
NM_004072.2:c.-3-12296G>T NP_004063.1:n.-3-12296G>T
XM_017018820.2:c.-3-12296G>T XP_016874309.1:n.-3-12296G>T
NM_001142343.2:c.-73-11591G>T MANE Select NP_001135815.1:n.-73-11591G>T
NM_001142344.2:c.-73-11591G>T NP_001135816.1:n.-73-11591G>T
NM_004072.3:c.-3-12296G>T NP_004063.1:n.-3-12296G>T
NM_001142345.2:c.-73-11591G>T NP_001135817.1:n.-73-11591G>T