Canonical Allele Identifier: CA2242009755
Gene: MC1R HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919986T= , CM000678.2:g.89919986T= GRCh38
NC_000016.9:g.89986394T= , CM000678.1:g.89986394T= GRCh37
NC_000016.8:g.88513895T= NCBI36
NG_012026.1:g.7108T=
NG_027810.1:g.2978T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000555147.2:c.728T= MANE Select ENSP00000451605.1:p.Leu243=
ENST00000639847.1:c.728T= ENSP00000492011.1:p.Leu243=
ENST00000555147.1:c.728T= ENSP00000451605.1:p.Leu243=
ENST00000555427.1:c.728T= ENSP00000451760.1:p.Leu243=
ENST00000556922.1:c.728T= ENSP00000451560.1:p.Leu243=
NM_002386.3:c.728T= NP_002377.4:p.Leu243=
NM_002386.4:c.728T= MANE Select NP_002377.4:p.Leu243=