Canonical Allele Identifier: CA2695224047
Gene: MC1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919739dup , CM000678.2:g.89919739dup GRCh38
NC_000016.9:g.89986147dup , CM000678.1:g.89986147dup GRCh37
NC_000016.8:g.88513648dup NCBI36
NG_012026.1:g.6861dup
NG_027810.1:g.2731dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.481dup MANE Select ENSP00000451605.1:p.Ala161GlyfsTer?
ENST00000639847.1:c.481dup ENSP00000492011.1:p.Ala161GlyfsTer?
ENST00000555147.1:c.481dup ENSP00000451605.1:p.Ala161GlyfsTer?
ENST00000555427.1:c.481dup ENSP00000451760.1:p.Ala161GlyfsTer?
ENST00000556922.1:c.481dup ENSP00000451560.1:p.Ala161GlyfsTer?
NM_002386.3:c.481dup NP_002377.4:p.Ala161GlyfsTer?
NM_002386.4:c.481dup MANE Select NP_002377.4:p.Ala161GlyfsTer?