Canonical Allele Identifier: CA1845591653
Gene: DNAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517336C= , CM000671.2:g.34517336C= GRCh38
NC_000009.11:g.34517334C= , CM000671.1:g.34517334C= GRCh37
NC_000009.10:g.34507334C= NCBI36
NG_008127.1:g.63524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1870C= MANE Select ENSP00000242317.4:p.Pro624=
ENST00000242317.8:c.1870C= ENSP00000242317.4:p.Pro624=
ENST00000442556.1:c.329+2597C=
ENST00000470169.5:c.658C=
ENST00000485580.1:n.446C=
ENST00000614641.4:c.1882C= ENSP00000480538.1:p.Pro628=
NM_001281428.1:c.1882C= NP_001268357.1:p.Pro628=
NM_012144.3:c.1870C= NP_036276.1:p.Pro624=
XM_006716758.2:c.1339C= XP_006716821.1:p.Pro447=
XM_011517848.1:c.1624C= XP_011516150.1:p.Pro542=
XM_006716758.3:c.1339C= XP_006716821.1:p.Pro447=
XM_011517848.2:c.1624C= XP_011516150.1:p.Pro542=
XM_017014625.2:c.1612C= XP_016870114.1:p.Pro538=
XR_002956774.1:n.1973C=
NM_012144.4:c.1870C= MANE Select NP_036276.1:p.Pro624=
NM_001281428.2:c.1882C= NP_001268357.1:p.Pro628=