Canonical Allele Identifier: CA2340050179
Gene: IZUMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.48745393G= , CM000681.2:g.48745393G= GRCh38
NC_000019.9:g.49248650G= , CM000681.1:g.49248650G= GRCh37
NC_000019.8:g.53940462G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332955.7:c.236-105C= MANE Select ENSP00000327786.2:n.236-105C=
ENST00000332955.6:c.236-105C= ENSP00000327786.2:n.236-105C=
ENST00000595517.5:c.169-105C= ENSP00000471815.1:n.169-105C=
ENST00000595937.5:c.236-105C= ENSP00000470144.1:n.236-105C=
ENST00000597553.1:n.788C=
ENST00000602105.1:c.-104-105C= ENSP00000471134.1:n.-104-105C=
NM_182575.2:c.236-105C= NP_872381.2:n.236-105C=
XM_005258793.3:c.314-105C= XP_005258850.1:n.314-105C=
XM_005258797.3:c.-104-105C= XP_005258854.1:n.-104-105C=
XM_005258798.3:c.-104-105C= XP_005258855.1:n.-104-105C=
XM_011526811.1:c.335-105C= XP_011525113.1:n.335-105C=
XM_011526812.1:c.236-105C= XP_011525114.1:n.236-105C=
XM_011526813.1:c.236-105C= XP_011525115.1:n.236-105C=
XM_011526814.1:c.43+89C= XP_011525116.1:n.43+89C=
XM_011526815.1:c.-105+93C= XP_011525117.1:n.-105+93C=
XM_011526816.1:c.-104-105C= XP_011525118.1:n.-104-105C=
XM_011526817.1:c.-104-105C= XP_011525119.1:n.-104-105C=
XR_243923.2:n.1249-105C=
XR_430196.2:n.1249-105C=
XR_935799.1:n.1249-105C=
NM_001321864.1:c.-104-105C= NP_001308793.1:n.-104-105C=
NM_001321865.1:c.-324-105C= NP_001308794.1:n.-324-105C=
NR_135832.1:n.242-105C=
NM_182575.3:c.236-105C= MANE Select NP_872381.2:n.236-105C=