Canonical Allele Identifier: CA405644691
Gene: YIF1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38307694C>A , CM000681.2:g.38307694C>A GRCh38
NC_000019.9:g.38798334C>A , CM000681.1:g.38798334C>A GRCh37
NC_000019.8:g.43490174C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001039672.3:c.598G>T MANE Select NP_001034761.1:p.Glu200Ter
ENST00000339413.11:c.598G>T MANE Select ENSP00000343435.5:p.Glu200Ter
NM_001039671.2:c.553G>T NP_001034760.1:p.Glu185Ter
NM_001039671.3:c.553G>T NP_001034760.1:p.Glu185Ter
NM_001039672.2:c.598G>T NP_001034761.1:p.Glu200Ter
NM_001039673.2:c.589G>T NP_001034762.1:p.Glu197Ter
NM_001039673.3:c.589G>T NP_001034762.1:p.Glu197Ter
NM_001145461.1:c.547G>T NP_001138933.1:p.Glu183Ter
NM_001145461.2:c.547G>T NP_001138933.1:p.Glu183Ter
NM_001145462.1:c.505G>T NP_001138934.1:p.Glu169Ter
NM_001145462.2:c.505G>T NP_001138934.1:p.Glu169Ter
NM_001145463.1:c.589G>T NP_001138935.1:p.Glu197Ter
NM_001145463.2:c.589G>T NP_001138935.1:p.Glu197Ter
ENST00000329420.12:c.553G>T ENSP00000329559.7:p.Glu185Ter
ENST00000337679.12:c.589G>T ENSP00000337411.7:p.Glu197Ter
ENST00000339413.10:c.598G>T ENSP00000343435.5:p.Glu200Ter
ENST00000392124.7:c.505G>T ENSP00000375971.2:p.Glu169Ter
ENST00000585563.5:n.852G>T
ENST00000586319.5:n.278G>T
ENST00000588002.5:c.482-173G>T
ENST00000589247.1:c.547G>T ENSP00000468463.1:p.Glu183Ter
ENST00000589644.1:n.985G>T
ENST00000591755.5:c.589G>T ENSP00000465446.1:p.Glu197Ter
ENST00000591784.5:c.505G>T ENSP00000465230.1:p.Glu169Ter
ENST00000592246.5:c.400G>T ENSP00000467489.1:p.Glu134Ter
ENST00000592694.5:c.505G>T ENSP00000466428.1:p.Glu169Ter
XM_005259385.2:c.505G>T XP_005259442.1:p.Glu169Ter
XM_005259385.4:c.505G>T XP_005259442.1:p.Glu169Ter
XM_011527467.1:c.589G>T XP_011525769.1:p.Glu197Ter
XM_017027449.1:c.589G>T XP_016882938.1:p.Glu197Ter
XM_017027450.1:c.598G>T XP_016882939.1:p.Glu200Ter
XM_017027451.1:c.553G>T XP_016882940.1:p.Glu185Ter