Canonical Allele Identifier: CA373244594
Gene: DNAI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34489365G>T , CM000671.2:g.34489365G>T GRCh38
NC_000009.11:g.34489363G>T , CM000671.1:g.34489363G>T GRCh37
NC_000009.10:g.34479363G>T NCBI36
NG_008127.1:g.35553G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.304G>T MANE Select ENSP00000242317.4:p.Val102Phe
ENST00000242317.8:c.304G>T ENSP00000242317.4:p.Val102Phe
ENST00000437363.5:c.271G>T ENSP00000395396.1:p.Val91Phe
ENST00000488369.1:n.420G>T
ENST00000614641.4:c.304G>T ENSP00000480538.1:p.Val102Phe
NM_001281428.1:c.304G>T NP_001268357.1:p.Val102Phe
NM_012144.3:c.304G>T NP_036276.1:p.Val102Phe
XM_011517846.1:c.304G>T XP_011516148.1:p.Val102Phe
XM_011517847.1:c.304G>T XP_011516149.1:p.Val102Phe
XM_011517848.1:c.304G>T XP_011516150.1:p.Val102Phe
XM_011517849.1:c.304G>T XP_011516151.1:p.Val102Phe
XM_011517850.1:c.304G>T XP_011516152.1:p.Val102Phe
XR_929232.1:n.558G>T
XR_929233.1:n.558G>T
XR_929235.1:n.558G>T
XM_006716758.3:c.-173G>T XP_006716821.1:n.-173G>T
XM_011517846.2:c.304G>T XP_011516148.1:p.Val102Phe
XM_011517847.3:c.304G>T XP_011516149.1:p.Val102Phe
XM_011517848.2:c.304G>T XP_011516150.1:p.Val102Phe
XM_011517849.2:c.304G>T XP_011516151.1:p.Val102Phe
XM_011517850.3:c.304G>T XP_011516152.1:p.Val102Phe
XM_017014625.2:c.304G>T XP_016870114.1:p.Val102Phe
XR_002956774.1:n.505G>T
XR_929232.2:n.505G>T
XR_929233.2:n.505G>T
NM_012144.4:c.304G>T MANE Select NP_036276.1:p.Val102Phe
NM_001281428.2:c.304G>T NP_001268357.1:p.Val102Phe