Canonical Allele Identifier: CA2340050235
Gene: IZUMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48745480A= , CM000681.2:g.48745480A= GRCh38
NC_000019.9:g.49248737A= , CM000681.1:g.49248737A= GRCh37
NC_000019.8:g.53940549A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332955.7:c.235+145T= MANE Select ENSP00000327786.2:n.235+145T=
ENST00000332955.6:c.235+145T= ENSP00000327786.2:n.235+145T=
ENST00000595517.5:c.169-192T= ENSP00000471815.1:n.169-192T=
ENST00000595937.5:c.235+145T= ENSP00000470144.1:n.235+145T=
ENST00000597553.1:n.701T=
ENST00000602105.1:c.-104-192T= ENSP00000471134.1:n.-104-192T=
NM_182575.2:c.235+145T= NP_872381.2:n.235+145T=
XM_005258793.3:c.313+145T= XP_005258850.1:n.313+145T=
XM_005258797.3:c.-104-192T= XP_005258854.1:n.-104-192T=
XM_005258798.3:c.-104-192T= XP_005258855.1:n.-104-192T=
XM_011526811.1:c.334+145T= XP_011525113.1:n.334+145T=
XM_011526812.1:c.235+145T= XP_011525114.1:n.235+145T=
XM_011526813.1:c.235+145T= XP_011525115.1:n.235+145T=
XM_011526814.1:c.43+2T= XP_011525116.1:n.43+2T=
XM_011526815.1:c.-105+6T= XP_011525117.1:n.-105+6T=
XM_011526816.1:c.-104-192T= XP_011525118.1:n.-104-192T=
XM_011526817.1:c.-104-192T= XP_011525119.1:n.-104-192T=
XR_243923.2:n.1248+145T=
XR_430196.2:n.1248+145T=
XR_935799.1:n.1248+145T=
NM_001321864.1:c.-104-192T= NP_001308793.1:n.-104-192T=
NM_001321865.1:c.-325+145T= NP_001308794.1:n.-325+145T=
NR_135832.1:n.242-192T=
NM_182575.3:c.235+145T= MANE Select NP_872381.2:n.235+145T=