Canonical Allele Identifier: CA1763389355
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622530T= , CM000670.2:g.10622530T= GRCh38
NC_000008.10:g.10480040T= , CM000670.1:g.10480040T= GRCh37
NC_000008.9:g.10517450T= NCBI36
NG_028035.1:g.37578A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.609+63A= MANE Select ENSP00000371923.3:n.609+63A=
ENST00000329335.3:n.859+63A=
ENST00000382483.3:c.609+63A= ENSP00000371923.3:n.609+63A=
NM_178857.5:c.609+63A= NP_849188.4:n.609+63A=
NM_178857.6:c.609+63A= MANE Select NP_849188.4:n.609+63A=