Canonical Allele Identifier: CA2733059078
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs2144391430

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919541_89919543del , CM000678.2:g.89919541_89919543del GRCh38
NC_000016.9:g.89985949_89985951del , CM000678.1:g.89985949_89985951del GRCh37
NC_000016.8:g.88513450_88513452del NCBI36
NG_012026.1:g.6663_6665del
NG_027810.1:g.2533_2535del

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.283_285del MANE Select ENSP00000451605.1:p.Thr95del
ENST00000639847.1:c.283_285del ENSP00000492011.1:p.Thr95del
ENST00000555147.1:c.283_285del ENSP00000451605.1:p.Thr95del
ENST00000555427.1:c.283_285del ENSP00000451760.1:p.Thr95del
ENST00000556922.1:c.283_285del ENSP00000451560.1:p.Thr95del
NM_002386.3:c.283_285del NP_002377.4:p.Thr95del
NM_002386.4:c.283_285del MANE Select NP_002377.4:p.Thr95del