Canonical Allele Identifier: CA1845608673

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34513119C= , CM000671.2:g.34513119C=	GRCh38
NC_000009.11:g.34513117C= , CM000671.1:g.34513117C=	GRCh37
NC_000009.10:g.34503117C=	NCBI36
NG_008127.1:g.59307C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1497C= MANE Select	ENSP00000242317.4:p.Gly499=
ENST00000242317.8:c.1497C=	ENSP00000242317.4:p.Gly499=
ENST00000442556.1:c.8C=
ENST00000470169.5:c.434C=
ENST00000614641.4:c.1509C=	ENSP00000480538.1:p.Gly503=
NM_001281428.1:c.1509C=	NP_001268357.1:p.Gly503=
NM_012144.3:c.1497C=	NP_036276.1:p.Gly499=
XM_006716758.2:c.966C=	XP_006716821.1:p.Gly322=
XM_011517846.1:c.1509C=	XP_011516148.1:p.Gly503=
XM_011517847.1:c.1509C=	XP_011516149.1:p.Gly503=
XM_011517848.1:c.1324-1275C=	XP_011516150.1:n.1324-1275C=
XM_011517849.1:c.1509C=	XP_011516151.1:p.Gly503=
XR_929232.1:n.1763C=
XR_929233.1:n.1763C=
XR_929235.1:n.1578-1385C=
XM_006716758.3:c.966C=	XP_006716821.1:p.Gly322=
XM_011517846.2:c.1509C=	XP_011516148.1:p.Gly503=
XM_011517847.3:c.1509C=	XP_011516149.1:p.Gly503=
XM_011517848.2:c.1324-1275C=	XP_011516150.1:n.1324-1275C=
XM_011517849.2:c.1509C=	XP_011516151.1:p.Gly503=
XM_017014625.2:c.1312-1275C=	XP_016870114.1:n.1312-1275C=
XR_002956774.1:n.1710C=
XR_929232.2:n.1710C=
XR_929233.2:n.1710C=
NM_012144.4:c.1497C= MANE Select	NP_036276.1:p.Gly499=
NM_001281428.2:c.1509C=	NP_001268357.1:p.Gly503=