Canonical Allele Identifier: CA2719565775
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs2132086187

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517098A>T , CM000671.2:g.34517098A>T GRCh38
NC_000009.11:g.34517096A>T , CM000671.1:g.34517096A>T GRCh37
NC_000009.10:g.34507096A>T NCBI36
NG_008127.1:g.63286A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1819-187A>T MANE Select ENSP00000242317.4:n.1819-187A>T
ENST00000242317.8:c.1819-187A>T ENSP00000242317.4:n.1819-187A>T
ENST00000442556.1:c.329+2359A>T
ENST00000470169.5:c.607-187A>T
ENST00000485580.1:n.395-187A>T
ENST00000614641.4:c.1831-187A>T ENSP00000480538.1:n.1831-187A>T
NM_001281428.1:c.1831-187A>T NP_001268357.1:n.1831-187A>T
NM_012144.3:c.1819-187A>T NP_036276.1:n.1819-187A>T
XM_006716758.2:c.1288-187A>T XP_006716821.1:n.1288-187A>T
XM_011517847.1:c.1831-97A>T XP_011516149.1:n.1831-97A>T
XM_011517848.1:c.1573-187A>T XP_011516150.1:n.1573-187A>T
XR_929233.1:n.1975-97A>T
XM_006716758.3:c.1288-187A>T XP_006716821.1:n.1288-187A>T
XM_011517847.3:c.1831-97A>T XP_011516149.1:n.1831-97A>T
XM_011517848.2:c.1573-187A>T XP_011516150.1:n.1573-187A>T
XM_017014625.2:c.1561-187A>T XP_016870114.1:n.1561-187A>T
XR_002956774.1:n.1922-187A>T
XR_929233.2:n.1922-97A>T
NM_012144.4:c.1819-187A>T MANE Select NP_036276.1:n.1819-187A>T
NM_001281428.2:c.1831-187A>T NP_001268357.1:n.1831-187A>T