Canonical Allele Identifier: CA1763378847
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10612668T= , CM000670.2:g.10612668T= GRCh38
NC_000008.10:g.10470178T= , CM000670.1:g.10470178T= GRCh37
NC_000008.9:g.10507588T= NCBI36
NG_028035.1:g.47440A=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.1430A= MANE Select ENSP00000371923.3:p.Glu477=
ENST00000382483.3:c.1430A= ENSP00000371923.3:p.Glu477=
NM_178857.5:c.1430A= NP_849188.4:p.Glu477=
NM_178857.6:c.1430A= MANE Select NP_849188.4:p.Glu477=