Canonical Allele Identifier: CA373244507
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489354A>G , CM000671.2:g.34489354A>G GRCh38
NC_000009.11:g.34489352A>G , CM000671.1:g.34489352A>G GRCh37
NC_000009.10:g.34479352A>G NCBI36
NG_008127.1:g.35542A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000242317.9:c.293A>G MANE Select ENSP00000242317.4:p.Asn98Ser
ENST00000242317.8:c.293A>G ENSP00000242317.4:p.Asn98Ser
ENST00000437363.5:c.260A>G ENSP00000395396.1:p.Asn87Ser
ENST00000488369.1:n.409A>G
ENST00000614641.4:c.293A>G ENSP00000480538.1:p.Asn98Ser
NM_001281428.1:c.293A>G NP_001268357.1:p.Asn98Ser
NM_012144.3:c.293A>G NP_036276.1:p.Asn98Ser
XM_011517846.1:c.293A>G XP_011516148.1:p.Asn98Ser
XM_011517847.1:c.293A>G XP_011516149.1:p.Asn98Ser
XM_011517848.1:c.293A>G XP_011516150.1:p.Asn98Ser
XM_011517849.1:c.293A>G XP_011516151.1:p.Asn98Ser
XM_011517850.1:c.293A>G XP_011516152.1:p.Asn98Ser
XR_929232.1:n.547A>G
XR_929233.1:n.547A>G
XR_929235.1:n.547A>G
XM_006716758.3:c.-184A>G XP_006716821.1:n.-184A>G
XM_011517846.2:c.293A>G XP_011516148.1:p.Asn98Ser
XM_011517847.3:c.293A>G XP_011516149.1:p.Asn98Ser
XM_011517848.2:c.293A>G XP_011516150.1:p.Asn98Ser
XM_011517849.2:c.293A>G XP_011516151.1:p.Asn98Ser
XM_011517850.3:c.293A>G XP_011516152.1:p.Asn98Ser
XM_017014625.2:c.293A>G XP_016870114.1:p.Asn98Ser
XR_002956774.1:n.494A>G
XR_929232.2:n.494A>G
XR_929233.2:n.494A>G
NM_012144.4:c.293A>G MANE Select NP_036276.1:p.Asn98Ser
NM_001281428.2:c.293A>G NP_001268357.1:p.Asn98Ser