Canonical Allele Identifier: CA2689798642
Gene: DNAI1 HGNC NCBI

Linked Data

gnomAD v4: 9-34517220-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517220C>A , CM000671.2:g.34517220C>A GRCh38
NC_000009.11:g.34517218C>A , CM000671.1:g.34517218C>A GRCh37
NC_000009.10:g.34507218C>A NCBI36
NG_008127.1:g.63408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-65C>A MANE Select ENSP00000242317.4:n.1819-65C>A
ENST00000242317.8:c.1819-65C>A ENSP00000242317.4:n.1819-65C>A
ENST00000442556.1:c.329+2481C>A
ENST00000470169.5:c.607-65C>A
ENST00000485580.1:n.395-65C>A
ENST00000614641.4:c.1831-65C>A ENSP00000480538.1:n.1831-65C>A
NM_001281428.1:c.1831-65C>A NP_001268357.1:n.1831-65C>A
NM_012144.3:c.1819-65C>A NP_036276.1:n.1819-65C>A
XM_006716758.2:c.1288-65C>A XP_006716821.1:n.1288-65C>A
XM_011517847.1:c.1856C>A XP_011516149.1:p.Ser619Ter
XM_011517848.1:c.1573-65C>A XP_011516150.1:n.1573-65C>A
XR_929233.1:n.2000C>A
XM_006716758.3:c.1288-65C>A XP_006716821.1:n.1288-65C>A
XM_011517847.3:c.1856C>A XP_011516149.1:p.Ser619Ter
XM_011517848.2:c.1573-65C>A XP_011516150.1:n.1573-65C>A
XM_017014625.2:c.1561-65C>A XP_016870114.1:n.1561-65C>A
XR_002956774.1:n.1922-65C>A
XR_929233.2:n.1947C>A
NM_012144.4:c.1819-65C>A MANE Select NP_036276.1:n.1819-65C>A
NM_001281428.2:c.1831-65C>A NP_001268357.1:n.1831-65C>A