Canonical Allele Identifier: CA1871446116
Gene: FRRS1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.109141468_109141470dup , CM000671.2:g.109141468_109141470dup GRCh38
NC_000009.11:g.111903748_111903750dup , CM000671.1:g.111903748_111903750dup GRCh37
NC_000009.10:g.110943569_110943571dup NCBI36
NG_051235.1:g.30824_30826dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000561981.5:c.584_586dup MANE Select ENSP00000477141.2:p.Gly195_Val196insGly
ENST00000642157.1:n.2819_2821dup
ENST00000644736.1:c.581_583dup
ENST00000644747.1:c.364_366dup ENSP00000493964.1:n.364_366dup
ENST00000645180.1:n.1335_1337dup
ENST00000561981.2:c.737_739dup ENSP00000477141.1:p.Gly246_Val247insGly
NM_014334.2:c.737_739dup NP_055149.2:p.Gly246_Val247insGly
XM_011518453.1:c.389_391dup XP_011516755.1:p.Gly130_Val131insGly
XM_011518454.1:c.389_391dup XP_011516756.1:p.Gly130_Val131insGly
NM_014334.3:c.737_739dup NP_055149.2:p.Gly246_Val247insGly
XM_011518454.3:c.389_391dup XP_011516756.1:p.Gly130_Val131insGly
NM_014334.4:c.584_586dup MANE Select NP_055149.3:p.Gly195_Val196insGly