Canonical Allele Identifier: CA980491112
Gene: MC1R HGNC NCBI

Linked Data

dbSNP Id: rs2045696533

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89919694_89919696del , CM000678.2:g.89919694_89919696del GRCh38
NC_000016.9:g.89986102_89986104del , CM000678.1:g.89986102_89986104del GRCh37
NC_000016.8:g.88513603_88513605del NCBI36
NG_012026.1:g.6816_6818del
NG_027810.1:g.2686_2688del

Transcript Alleles

HGVS Amino-acid change
ENST00000555147.2:c.436_438del MANE Select ENSP00000451605.1:p.Ile146del
ENST00000639847.1:c.436_438del ENSP00000492011.1:p.Ile146del
ENST00000555147.1:c.436_438del ENSP00000451605.1:p.Ile146del
ENST00000555427.1:c.436_438del ENSP00000451760.1:p.Ile146del
ENST00000556922.1:c.436_438del ENSP00000451560.1:p.Ile146del
NM_002386.3:c.436_438del NP_002377.4:p.Ile146del
NM_002386.4:c.436_438del MANE Select NP_002377.4:p.Ile146del