Canonical Allele Identifier: CA2560622

Gene: RABL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.120730727G>T , CM000665.2:g.120730727G>T	GRCh38
NC_000003.11:g.120449574G>T , CM000665.1:g.120449574G>T	GRCh37
NC_000003.10:g.121932264G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273375.8:c.107C>A MANE Select	ENSP00000273375.4:p.Ser36Ter
ENST00000648525.1:n.234C>A
ENST00000273375.7:c.107C>A	ENSP00000273375.3:p.Ser36Ter
ENST00000465022.5:c.107C>A	ENSP00000420573.1:p.Ser36Ter
ENST00000473654.5:c.107C>A	ENSP00000419310.1:p.Ser36Ter
ENST00000481015.5:c.105C>A
ENST00000483733.1:c.107C>A	ENSP00000419986.1:p.Ser36Ter
ENST00000485161.5:c.107C>A	ENSP00000417266.1:p.Ser36Ter
ENST00000491398.5:n.274C>A
NM_173825.3:c.107C>A	NP_776186.2:p.Ser36Ter
XM_006713595.1:c.107C>A	XP_006713658.1:p.Ser36Ter
NM_001363964.1:c.107C>A	NP_001350893.1:p.Ser36Ter
NM_001363965.1:c.107C>A	NP_001350894.1:p.Ser36Ter
NM_173825.4:c.107C>A	NP_776186.2:p.Ser36Ter
NR_157022.1:n.421C>A
XM_017006228.2:c.107C>A	XP_016861717.1:p.Ser36Ter
NM_173825.5:c.107C>A MANE Select	NP_776186.2:p.Ser36Ter