Canonical Allele Identifier: CA1845608793

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34513165G= , CM000671.2:g.34513165G=	GRCh38
NC_000009.11:g.34513163G= , CM000671.1:g.34513163G=	GRCh37
NC_000009.10:g.34503163G=	NCBI36
NG_008127.1:g.59353G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1543G= MANE Select	ENSP00000242317.4:p.Gly515=
ENST00000242317.8:c.1543G=	ENSP00000242317.4:p.Gly515=
ENST00000442556.1:c.54G=
ENST00000470169.5:c.480G=
ENST00000485580.1:n.22G=
ENST00000614641.4:c.1555G=	ENSP00000480538.1:p.Gly519=
NM_001281428.1:c.1555G=	NP_001268357.1:p.Gly519=
NM_012144.3:c.1543G=	NP_036276.1:p.Gly515=
XM_006716758.2:c.1012G=	XP_006716821.1:p.Gly338=
XM_011517846.1:c.1555G=	XP_011516148.1:p.Gly519=
XM_011517847.1:c.1555G=	XP_011516149.1:p.Gly519=
XM_011517848.1:c.1324-1229G=	XP_011516150.1:n.1324-1229G=
XM_011517849.1:c.1555G=	XP_011516151.1:p.Gly519=
XR_929232.1:n.1809G=
XR_929233.1:n.1809G=
XR_929235.1:n.1578-1339G=
XM_006716758.3:c.1012G=	XP_006716821.1:p.Gly338=
XM_011517846.2:c.1555G=	XP_011516148.1:p.Gly519=
XM_011517847.3:c.1555G=	XP_011516149.1:p.Gly519=
XM_011517848.2:c.1324-1229G=	XP_011516150.1:n.1324-1229G=
XM_011517849.2:c.1555G=	XP_011516151.1:p.Gly519=
XM_017014625.2:c.1312-1229G=	XP_016870114.1:n.1312-1229G=
XR_002956774.1:n.1756G=
XR_929232.2:n.1756G=
XR_929233.2:n.1756G=
NM_012144.4:c.1543G= MANE Select	NP_036276.1:p.Gly515=
NM_001281428.2:c.1555G=	NP_001268357.1:p.Gly519=