Canonical Allele Identifier: CA373264010
Community Standard Title: NM_012144.4(DNAI1):c.1718+1G>A
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34514543G>A , CM000671.2:g.34514543G>A GRCh38
NC_000009.11:g.34514541G>A , CM000671.1:g.34514541G>A GRCh37
NC_000009.10:g.34504541G>A NCBI36
NG_008127.1:g.60731G>A

Transcript Alleles

HGVS Amino-acid Change
NM_012144.4:c.1718+1G>A MANE Select NP_036276.1:n.1718+1G>A
ENST00000242317.9:c.1718+1G>A MANE Select ENSP00000242317.4:n.1718+1G>A
NM_001281428.1:c.1730+1G>A NP_001268357.1:n.1730+1G>A
NM_001281428.2:c.1730+1G>A NP_001268357.1:n.1730+1G>A
NM_012144.3:c.1718+1G>A NP_036276.1:n.1718+1G>A
ENST00000242317.8:c.1718+1G>A ENSP00000242317.4:n.1718+1G>A
ENST00000442556.1:c.229+1G>A
ENST00000470169.5:c.507-97G>A
ENST00000485580.1:n.198G>A
ENST00000614641.4:c.1730+1G>A ENSP00000480538.1:n.1730+1G>A
XM_006716758.2:c.1187+1G>A XP_006716821.1:n.1187+1G>A
XM_006716758.3:c.1187+1G>A XP_006716821.1:n.1187+1G>A
XM_011517846.1:c.1730+1G>A XP_011516148.1:n.1730+1G>A
XM_011517846.2:c.1730+1G>A XP_011516148.1:n.1730+1G>A
XM_011517847.1:c.1730+1G>A XP_011516149.1:n.1730+1G>A
XM_011517847.3:c.1730+1G>A XP_011516149.1:n.1730+1G>A
XM_011517848.1:c.1472+1G>A XP_011516150.1:n.1472+1G>A
XM_011517848.2:c.1472+1G>A XP_011516150.1:n.1472+1G>A
XM_011517849.1:c.1620+1G>A XP_011516151.1:n.1620+1G>A
XM_011517849.2:c.1620+1G>A XP_011516151.1:n.1620+1G>A
XM_017014625.2:c.1460+1G>A XP_016870114.1:n.1460+1G>A
XR_002956774.1:n.1821+1G>A
XR_929232.1:n.1874+1G>A
XR_929232.2:n.1821+1G>A
XR_929233.1:n.1874+1G>A
XR_929233.2:n.1821+1G>A
XR_929235.1:n.1616+1G>A