Canonical Allele Identifier: CA2340050237
Gene: IZUMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48745484G= , CM000681.2:g.48745484G= GRCh38
NC_000019.9:g.49248741G= , CM000681.1:g.49248741G= GRCh37
NC_000019.8:g.53940553G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332955.7:c.235+141C= MANE Select ENSP00000327786.2:n.235+141C=
ENST00000332955.6:c.235+141C= ENSP00000327786.2:n.235+141C=
ENST00000595517.5:c.169-196C= ENSP00000471815.1:n.169-196C=
ENST00000595937.5:c.235+141C= ENSP00000470144.1:n.235+141C=
ENST00000597553.1:n.697C=
ENST00000602105.1:c.-104-196C= ENSP00000471134.1:n.-104-196C=
NM_182575.2:c.235+141C= NP_872381.2:n.235+141C=
XM_005258793.3:c.313+141C= XP_005258850.1:n.313+141C=
XM_005258797.3:c.-104-196C= XP_005258854.1:n.-104-196C=
XM_005258798.3:c.-104-196C= XP_005258855.1:n.-104-196C=
XM_011526811.1:c.334+141C= XP_011525113.1:n.334+141C=
XM_011526812.1:c.235+141C= XP_011525114.1:n.235+141C=
XM_011526813.1:c.235+141C= XP_011525115.1:n.235+141C=
XM_011526814.1:c.41C= XP_011525116.1:p.Ala14=
XM_011526815.1:c.-105+2C= XP_011525117.1:n.-105+2C=
XM_011526816.1:c.-104-196C= XP_011525118.1:n.-104-196C=
XM_011526817.1:c.-104-196C= XP_011525119.1:n.-104-196C=
XR_243923.2:n.1248+141C=
XR_430196.2:n.1248+141C=
XR_935799.1:n.1248+141C=
NM_001321864.1:c.-104-196C= NP_001308793.1:n.-104-196C=
NM_001321865.1:c.-325+141C= NP_001308794.1:n.-325+141C=
NR_135832.1:n.242-196C=
NM_182575.3:c.235+141C= MANE Select NP_872381.2:n.235+141C=