Canonical Allele Identifier: CA2285919172
Gene: MC2R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884606_13884612delinsAAACCAG , CM000680.2:g.13884606_13884612delinsAAACCAG GRCh38
NC_000018.9:g.13884605_13884611delinsAAACCAG , CM000680.1:g.13884605_13884611delinsAAACCAG GRCh37
NC_000018.8:g.13874605_13874611delinsAAACCAG NCBI36
NG_011819.1:g.35925_35931delinsCTGGTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.*13_*19delinsCTGGTTT MANE Select ENSP00000333821.2:n.*13_*19delinsCTGGTTT
ENST00000327606.3:c.*13_*19delinsCTGGTTT ENSP00000333821.2:n.*13_*19delinsCTGGTTT
NM_000529.2:c.*13_*19delinsCTGGTTT MANE Select NP_000520.1:n.*13_*19delinsCTGGTTT
NM_001291911.1:c.*13_*19delinsCTGGTTT NP_001278840.1:n.*13_*19delinsCTGGTTT
XM_017025781.1:c.*13_*19delinsCTGGTTT XP_016881270.1:n.*13_*19delinsCTGGTTT