Canonical Allele Identifier: CA459618832
Gene: RP1L1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.10468542T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10611032T>A , CM000670.2:g.10611032T>A GRCh38
NC_000008.10:g.10468542T>A , CM000670.1:g.10468542T>A GRCh37
NC_000008.9:g.10505952T>A NCBI36
NG_028035.1:g.49076A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382483.4:c.3066A>T MANE Select ENSP00000371923.3:p.Pro1022=
ENST00000382483.3:c.3066A>T ENSP00000371923.3:p.Pro1022=
NM_178857.5:c.3066A>T NP_849188.4:p.Pro1022=
NM_178857.6:c.3066A>T MANE Select NP_849188.4:p.Pro1022=