Canonical Allele Identifier: CA5034567
Gene: DNAI1 HGNC NCBI

Linked Data

dbSNP Id: rs142404489
gnomAD v2: 9-34517335-C-T
gnomAD v3: 9-34517337-C-T
gnomAD v4: 9-34517337-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.34517337C>T , CM000671.2:g.34517337C>T GRCh38
NC_000009.11:g.34517335C>T , CM000671.1:g.34517335C>T GRCh37
NC_000009.10:g.34507335C>T NCBI36
NG_008127.1:g.63525C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000242317.9:c.1871C>T MANE Select ENSP00000242317.4:p.Pro624Leu
ENST00000242317.8:c.1871C>T ENSP00000242317.4:p.Pro624Leu
ENST00000442556.1:c.329+2598C>T
ENST00000470169.5:c.659C>T
ENST00000485580.1:n.447C>T
ENST00000614641.4:c.1883C>T ENSP00000480538.1:p.Pro628Leu
NM_001281428.1:c.1883C>T NP_001268357.1:p.Pro628Leu
NM_012144.3:c.1871C>T NP_036276.1:p.Pro624Leu
XM_006716758.2:c.1340C>T XP_006716821.1:p.Pro447Leu
XM_011517848.1:c.1625C>T XP_011516150.1:p.Pro542Leu
XM_006716758.3:c.1340C>T XP_006716821.1:p.Pro447Leu
XM_011517848.2:c.1625C>T XP_011516150.1:p.Pro542Leu
XM_017014625.2:c.1613C>T XP_016870114.1:p.Pro538Leu
XR_002956774.1:n.1974C>T
NM_012144.4:c.1871C>T MANE Select NP_036276.1:p.Pro624Leu
NM_001281428.2:c.1883C>T NP_001268357.1:p.Pro628Leu