Canonical Allele Identifier: CA1845591532

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517291A= , CM000671.2:g.34517291A=	GRCh38
NC_000009.11:g.34517289A= , CM000671.1:g.34517289A=	GRCh37
NC_000009.10:g.34507289A=	NCBI36
NG_008127.1:g.63479A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1825A= MANE Select	ENSP00000242317.4:p.Ile609=
ENST00000242317.8:c.1825A=	ENSP00000242317.4:p.Ile609=
ENST00000442556.1:c.329+2552A=
ENST00000470169.5:c.613A=
ENST00000485580.1:n.401A=
ENST00000614641.4:c.1837A=	ENSP00000480538.1:p.Ile613=
NM_001281428.1:c.1837A=	NP_001268357.1:p.Ile613=
NM_012144.3:c.1825A=	NP_036276.1:p.Ile609=
XM_006716758.2:c.1294A=	XP_006716821.1:p.Ile432=
XM_011517848.1:c.1579A=	XP_011516150.1:p.Ile527=
XM_006716758.3:c.1294A=	XP_006716821.1:p.Ile432=
XM_011517848.2:c.1579A=	XP_011516150.1:p.Ile527=
XM_017014625.2:c.1567A=	XP_016870114.1:p.Ile523=
XR_002956774.1:n.1928A=
NM_012144.4:c.1825A= MANE Select	NP_036276.1:p.Ile609=
NM_001281428.2:c.1837A=	NP_001268357.1:p.Ile613=