Canonical Allele Identifier: CA2641150774
Gene: MC2R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.13884778_13884780del , CM000680.2:g.13884778_13884780del GRCh38
NC_000018.9:g.13884777_13884779del , CM000680.1:g.13884777_13884779del GRCh37
NC_000018.8:g.13874777_13874779del NCBI36
NG_011819.1:g.35758_35760del

Transcript Alleles

HGVS Amino-acid change
ENST00000327606.4:c.740_742del MANE Select ENSP00000333821.2:p.Ser247del
ENST00000327606.3:c.740_742del ENSP00000333821.2:p.Ser247del
NM_000529.2:c.740_742del MANE Select NP_000520.1:p.Ser247del
NM_001291911.1:c.740_742del NP_001278840.1:p.Ser247del
XM_017025781.1:c.740_742del XP_016881270.1:p.Ser247del