Canonical Allele Identifier: CA373266433
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517315T>A , CM000671.2:g.34517315T>A GRCh38
NC_000009.11:g.34517313T>A , CM000671.1:g.34517313T>A GRCh37
NC_000009.10:g.34507313T>A NCBI36
NG_008127.1:g.63503T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1849T>A MANE Select ENSP00000242317.4:p.Tyr617Asn
ENST00000242317.8:c.1849T>A ENSP00000242317.4:p.Tyr617Asn
ENST00000442556.1:c.329+2576T>A
ENST00000470169.5:c.637T>A
ENST00000485580.1:n.425T>A
ENST00000614641.4:c.1861T>A ENSP00000480538.1:p.Tyr621Asn
NM_001281428.1:c.1861T>A NP_001268357.1:p.Tyr621Asn
NM_012144.3:c.1849T>A NP_036276.1:p.Tyr617Asn
XM_006716758.2:c.1318T>A XP_006716821.1:p.Tyr440Asn
XM_011517848.1:c.1603T>A XP_011516150.1:p.Tyr535Asn
XM_006716758.3:c.1318T>A XP_006716821.1:p.Tyr440Asn
XM_011517848.2:c.1603T>A XP_011516150.1:p.Tyr535Asn
XM_017014625.2:c.1591T>A XP_016870114.1:p.Tyr531Asn
XR_002956774.1:n.1952T>A
NM_012144.4:c.1849T>A MANE Select NP_036276.1:p.Tyr617Asn
NM_001281428.2:c.1861T>A NP_001268357.1:p.Tyr621Asn