Canonical Allele Identifier: CA1845574647

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34489350G= , CM000671.2:g.34489350G=	GRCh38
NC_000009.11:g.34489348G= , CM000671.1:g.34489348G=	GRCh37
NC_000009.10:g.34479348G=	NCBI36
NG_008127.1:g.35538G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.289G= MANE Select	ENSP00000242317.4:p.Val97=
ENST00000242317.8:c.289G=	ENSP00000242317.4:p.Val97=
ENST00000437363.5:c.256G=	ENSP00000395396.1:p.Val86=
ENST00000488369.1:n.405G=
ENST00000614641.4:c.289G=	ENSP00000480538.1:p.Val97=
NM_001281428.1:c.289G=	NP_001268357.1:p.Val97=
NM_012144.3:c.289G=	NP_036276.1:p.Val97=
XM_011517846.1:c.289G=	XP_011516148.1:p.Val97=
XM_011517847.1:c.289G=	XP_011516149.1:p.Val97=
XM_011517848.1:c.289G=	XP_011516150.1:p.Val97=
XM_011517849.1:c.289G=	XP_011516151.1:p.Val97=
XM_011517850.1:c.289G=	XP_011516152.1:p.Val97=
XR_929232.1:n.543G=
XR_929233.1:n.543G=
XR_929235.1:n.543G=
XM_006716758.3:c.-188G=	XP_006716821.1:n.-188G=
XM_011517846.2:c.289G=	XP_011516148.1:p.Val97=
XM_011517847.3:c.289G=	XP_011516149.1:p.Val97=
XM_011517848.2:c.289G=	XP_011516150.1:p.Val97=
XM_011517849.2:c.289G=	XP_011516151.1:p.Val97=
XM_011517850.3:c.289G=	XP_011516152.1:p.Val97=
XM_017014625.2:c.289G=	XP_016870114.1:p.Val97=
XR_002956774.1:n.490G=
XR_929232.2:n.490G=
XR_929233.2:n.490G=
NM_012144.4:c.289G= MANE Select	NP_036276.1:p.Val97=
NM_001281428.2:c.289G=	NP_001268357.1:p.Val97=