Canonical Allele Identifier: CA1845591606

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517320G= , CM000671.2:g.34517320G=	GRCh38
NC_000009.11:g.34517318G= , CM000671.1:g.34517318G=	GRCh37
NC_000009.10:g.34507318G=	NCBI36
NG_008127.1:g.63508G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1854G= MANE Select	ENSP00000242317.4:p.Glu618=
ENST00000242317.8:c.1854G=	ENSP00000242317.4:p.Glu618=
ENST00000442556.1:c.329+2581G=
ENST00000470169.5:c.642G=
ENST00000485580.1:n.430G=
ENST00000614641.4:c.1866G=	ENSP00000480538.1:p.Glu622=
NM_001281428.1:c.1866G=	NP_001268357.1:p.Glu622=
NM_012144.3:c.1854G=	NP_036276.1:p.Glu618=
XM_006716758.2:c.1323G=	XP_006716821.1:p.Glu441=
XM_011517848.1:c.1608G=	XP_011516150.1:p.Glu536=
XM_006716758.3:c.1323G=	XP_006716821.1:p.Glu441=
XM_011517848.2:c.1608G=	XP_011516150.1:p.Glu536=
XM_017014625.2:c.1596G=	XP_016870114.1:p.Glu532=
XR_002956774.1:n.1957G=
NM_012144.4:c.1854G= MANE Select	NP_036276.1:p.Glu618=
NM_001281428.2:c.1866G=	NP_001268357.1:p.Glu622=