Canonical Allele Identifier: CA883051776
Gene: IZUMO1 HGNC NCBI

Linked Data

dbSNP Id: rs775318880

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48745486C>T , CM000681.2:g.48745486C>T GRCh38
NC_000019.9:g.49248743C>T , CM000681.1:g.49248743C>T GRCh37
NC_000019.8:g.53940555C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332955.7:c.235+139G>A MANE Select ENSP00000327786.2:n.235+139G>A
ENST00000332955.6:c.235+139G>A ENSP00000327786.2:n.235+139G>A
ENST00000595517.5:c.169-198G>A ENSP00000471815.1:n.169-198G>A
ENST00000595937.5:c.235+139G>A ENSP00000470144.1:n.235+139G>A
ENST00000597553.1:n.695G>A
ENST00000602105.1:c.-104-198G>A ENSP00000471134.1:n.-104-198G>A
NM_182575.2:c.235+139G>A NP_872381.2:n.235+139G>A
XM_005258793.3:c.313+139G>A XP_005258850.1:n.313+139G>A
XM_005258797.3:c.-104-198G>A XP_005258854.1:n.-104-198G>A
XM_005258798.3:c.-104-198G>A XP_005258855.1:n.-104-198G>A
XM_011526811.1:c.334+139G>A XP_011525113.1:n.334+139G>A
XM_011526812.1:c.235+139G>A XP_011525114.1:n.235+139G>A
XM_011526813.1:c.235+139G>A XP_011525115.1:n.235+139G>A
XM_011526814.1:c.39G>A XP_011525116.1:p.Glu13=
XM_011526815.1:c.-105G>A XP_011525117.1:n.-105G>A
XM_011526816.1:c.-104-198G>A XP_011525118.1:n.-104-198G>A
XM_011526817.1:c.-104-198G>A XP_011525119.1:n.-104-198G>A
XR_243923.2:n.1248+139G>A
XR_430196.2:n.1248+139G>A
XR_935799.1:n.1248+139G>A
NM_001321864.1:c.-104-198G>A NP_001308793.1:n.-104-198G>A
NM_001321865.1:c.-325+139G>A NP_001308794.1:n.-325+139G>A
NR_135832.1:n.242-198G>A
NM_182575.3:c.235+139G>A MANE Select NP_872381.2:n.235+139G>A