Canonical Allele Identifier: CA1763389835
Gene: RP1L1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10622782G= , CM000670.2:g.10622782G= GRCh38
NC_000008.10:g.10480292G= , CM000670.1:g.10480292G= GRCh37
NC_000008.9:g.10517702G= NCBI36
NG_028035.1:g.37326C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382483.4:c.420C= MANE Select ENSP00000371923.3:p.Gly140=
ENST00000329335.3:n.670C=
ENST00000382483.3:c.420C= ENSP00000371923.3:p.Gly140=
NM_178857.5:c.420C= NP_849188.4:p.Gly140=
NM_178857.6:c.420C= MANE Select NP_849188.4:p.Gly140=