Canonical Allele Identifier: CA2719566418
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs2132086725

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517484T>A , CM000671.2:g.34517484T>A GRCh38
NC_000009.11:g.34517482T>A , CM000671.1:g.34517482T>A GRCh37
NC_000009.10:g.34507482T>A NCBI36
NG_008127.1:g.63672T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000242317.9:c.2001+17T>A MANE Select ENSP00000242317.4:n.2001+17T>A
ENST00000242317.8:c.2001+17T>A ENSP00000242317.4:n.2001+17T>A
ENST00000442556.1:c.329+2745T>A
ENST00000614641.4:c.2013+17T>A ENSP00000480538.1:n.2013+17T>A
NM_001281428.1:c.2013+17T>A NP_001268357.1:n.2013+17T>A
NM_012144.3:c.2001+17T>A NP_036276.1:n.2001+17T>A
XM_006716758.2:c.1470+17T>A XP_006716821.1:n.1470+17T>A
XM_011517848.1:c.1755+17T>A XP_011516150.1:n.1755+17T>A
XM_006716758.3:c.1470+17T>A XP_006716821.1:n.1470+17T>A
XM_011517848.2:c.1755+17T>A XP_011516150.1:n.1755+17T>A
XM_017014625.2:c.1743+17T>A XP_016870114.1:n.1743+17T>A
XR_002956774.1:n.2104+17T>A
NM_012144.4:c.2001+17T>A MANE Select NP_036276.1:n.2001+17T>A
NM_001281428.2:c.2013+17T>A NP_001268357.1:n.2013+17T>A