Canonical Allele Identifier: CA8255718
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs760716521

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919972dup , CM000678.2:g.89919972dup GRCh38
NC_000016.9:g.89986380dup , CM000678.1:g.89986380dup GRCh37
NC_000016.8:g.88513881dup NCBI36
NG_012026.1:g.7094dup
NG_027810.1:g.2964dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.714dup MANE Select ENSP00000451605.1:p.Gly239ArgfsTer?
ENST00000639847.1:c.714dup ENSP00000492011.1:p.Gly239ArgfsTer?
ENST00000555147.1:c.714dup ENSP00000451605.1:p.Gly239ArgfsTer?
ENST00000555427.1:c.714dup ENSP00000451760.1:p.Gly239ArgfsTer?
ENST00000556922.1:c.714dup ENSP00000451560.1:p.Gly239ArgfsTer?
NM_002386.3:c.714dup NP_002377.4:p.Gly239ArgfsTer?
NM_002386.4:c.714dup MANE Select NP_002377.4:p.Gly239ArgfsTer?