Canonical Allele Identifier: CA2242009584
Gene: MC1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919745_89919756delinsCGAGCCGTTGCG , CM000678.2:g.89919745_89919756delinsCGAGCCGTTGCG GRCh38
NC_000016.9:g.89986153_89986164delinsCGAGCCGTTGCG , CM000678.1:g.89986153_89986164delinsCGAGCCGTTGCG GRCh37
NC_000016.8:g.88513654_88513665delinsCGAGCCGTTGCG NCBI36
NG_012026.1:g.6867_6878delinsCGAGCCGTTGCG
NG_027810.1:g.2737_2748delinsCGAGCCGTTGCG

Transcript Alleles

HGVS Amino-acid change
ENST00000555147.2:c.487_498delinsCGAGCCGTTGCG MANE Select ENSP00000451605.1:p.Arg163=
ENST00000639847.1:c.487_498delinsCGAGCCGTTGCG ENSP00000492011.1:p.Arg163=
ENST00000555147.1:c.487_498delinsCGAGCCGTTGCG ENSP00000451605.1:p.Arg163=
ENST00000555427.1:c.487_498delinsCGAGCCGTTGCG ENSP00000451760.1:p.Arg163=
ENST00000556922.1:c.487_498delinsCGAGCCGTTGCG ENSP00000451560.1:p.Arg163=
NM_002386.3:c.487_498delinsCGAGCCGTTGCG NP_002377.4:p.Arg163=
NM_002386.4:c.487_498delinsCGAGCCGTTGCG MANE Select NP_002377.4:p.Arg163=