Canonical Allele Identifier: CA373244560
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs894465418

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489360T>G , CM000671.2:g.34489360T>G GRCh38
NC_000009.11:g.34489358T>G , CM000671.1:g.34489358T>G GRCh37
NC_000009.10:g.34479358T>G NCBI36
NG_008127.1:g.35548T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.299T>G MANE Select ENSP00000242317.4:p.Leu100Arg
ENST00000242317.8:c.299T>G ENSP00000242317.4:p.Leu100Arg
ENST00000437363.5:c.266T>G ENSP00000395396.1:p.Leu89Arg
ENST00000488369.1:n.415T>G
ENST00000614641.4:c.299T>G ENSP00000480538.1:p.Leu100Arg
NM_001281428.1:c.299T>G NP_001268357.1:p.Leu100Arg
NM_012144.3:c.299T>G NP_036276.1:p.Leu100Arg
XM_011517846.1:c.299T>G XP_011516148.1:p.Leu100Arg
XM_011517847.1:c.299T>G XP_011516149.1:p.Leu100Arg
XM_011517848.1:c.299T>G XP_011516150.1:p.Leu100Arg
XM_011517849.1:c.299T>G XP_011516151.1:p.Leu100Arg
XM_011517850.1:c.299T>G XP_011516152.1:p.Leu100Arg
XR_929232.1:n.553T>G
XR_929233.1:n.553T>G
XR_929235.1:n.553T>G
XM_006716758.3:c.-178T>G XP_006716821.1:n.-178T>G
XM_011517846.2:c.299T>G XP_011516148.1:p.Leu100Arg
XM_011517847.3:c.299T>G XP_011516149.1:p.Leu100Arg
XM_011517848.2:c.299T>G XP_011516150.1:p.Leu100Arg
XM_011517849.2:c.299T>G XP_011516151.1:p.Leu100Arg
XM_011517850.3:c.299T>G XP_011516152.1:p.Leu100Arg
XM_017014625.2:c.299T>G XP_016870114.1:p.Leu100Arg
XR_002956774.1:n.500T>G
XR_929232.2:n.500T>G
XR_929233.2:n.500T>G
NM_012144.4:c.299T>G MANE Select NP_036276.1:p.Leu100Arg
NM_001281428.2:c.299T>G NP_001268357.1:p.Leu100Arg