Canonical Allele Identifier: CA1763383790
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10611035G= , CM000670.2:g.10611035G= GRCh38
NC_000008.10:g.10468545G= , CM000670.1:g.10468545G= GRCh37
NC_000008.9:g.10505955G= NCBI36
NG_028035.1:g.49073C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.3063C= MANE Select ENSP00000371923.3:p.Asp1021=
ENST00000382483.3:c.3063C= ENSP00000371923.3:p.Asp1021=
NM_178857.5:c.3063C= NP_849188.4:p.Asp1021=
NM_178857.6:c.3063C= MANE Select NP_849188.4:p.Asp1021=