Canonical Allele Identifier: CA1845591702

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517345G= , CM000671.2:g.34517345G=	GRCh38
NC_000009.11:g.34517343G= , CM000671.1:g.34517343G=	GRCh37
NC_000009.10:g.34507343G=	NCBI36
NG_008127.1:g.63533G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1879G= MANE Select	ENSP00000242317.4:p.Ala627=
ENST00000242317.8:c.1879G=	ENSP00000242317.4:p.Ala627=
ENST00000442556.1:c.329+2606G=
ENST00000470169.5:c.667G=
ENST00000485580.1:n.455G=
ENST00000614641.4:c.1891G=	ENSP00000480538.1:p.Ala631=
NM_001281428.1:c.1891G=	NP_001268357.1:p.Ala631=
NM_012144.3:c.1879G=	NP_036276.1:p.Ala627=
XM_006716758.2:c.1348G=	XP_006716821.1:p.Ala450=
XM_011517848.1:c.1633G=	XP_011516150.1:p.Ala545=
XM_006716758.3:c.1348G=	XP_006716821.1:p.Ala450=
XM_011517848.2:c.1633G=	XP_011516150.1:p.Ala545=
XM_017014625.2:c.1621G=	XP_016870114.1:p.Ala541=
XR_002956774.1:n.1982G=
NM_012144.4:c.1879G= MANE Select	NP_036276.1:p.Ala627=
NM_001281428.2:c.1891G=	NP_001268357.1:p.Ala631=