Canonical Allele Identifier: CA2635067119
Gene: MC1R HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919974_89919983del , CM000678.2:g.89919974_89919983del GRCh38
NC_000016.9:g.89986382_89986391del , CM000678.1:g.89986382_89986391del GRCh37
NC_000016.8:g.88513883_88513892del NCBI36
NG_012026.1:g.7096_7105del
NG_027810.1:g.2966_2975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.716_725del MANE Select ENSP00000451605.1:p.Gly239AlafsTer?
ENST00000639847.1:c.716_725del ENSP00000492011.1:p.Gly239AlafsTer?
ENST00000555147.1:c.716_725del ENSP00000451605.1:p.Gly239AlafsTer?
ENST00000555427.1:c.716_725del ENSP00000451760.1:p.Gly239AlafsTer?
ENST00000556922.1:c.716_725del ENSP00000451560.1:p.Gly239AlafsTer?
NM_002386.3:c.716_725del NP_002377.4:p.Gly239AlafsTer?
NM_002386.4:c.716_725del MANE Select NP_002377.4:p.Gly239AlafsTer?