Canonical Allele Identifier: CA1845610303

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514403T= , CM000671.2:g.34514403T=	GRCh38
NC_000009.11:g.34514401T= , CM000671.1:g.34514401T=	GRCh37
NC_000009.10:g.34504401T=	NCBI36
NG_008127.1:g.60591T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1579T= MANE Select	ENSP00000242317.4:p.Ser527=
ENST00000242317.8:c.1579T=	ENSP00000242317.4:p.Ser527=
ENST00000442556.1:c.90T=
ENST00000470169.5:c.507-237T=
ENST00000485580.1:n.58T=
ENST00000614641.4:c.1591T=	ENSP00000480538.1:p.Ser531=
NM_001281428.1:c.1591T=	NP_001268357.1:p.Ser531=
NM_012144.3:c.1579T=	NP_036276.1:p.Ser527=
XM_006716758.2:c.1048T=	XP_006716821.1:p.Ser350=
XM_011517846.1:c.1591T=	XP_011516148.1:p.Ser531=
XM_011517847.1:c.1591T=	XP_011516149.1:p.Ser531=
XM_011517848.1:c.1333T=	XP_011516150.1:p.Ser445=
XM_011517849.1:c.1582-101T=	XP_011516151.1:n.1582-101T=
XR_929232.1:n.1836-101T=
XR_929233.1:n.1836-101T=
XR_929235.1:n.1578-101T=
XM_006716758.3:c.1048T=	XP_006716821.1:p.Ser350=
XM_011517846.2:c.1591T=	XP_011516148.1:p.Ser531=
XM_011517847.3:c.1591T=	XP_011516149.1:p.Ser531=
XM_011517848.2:c.1333T=	XP_011516150.1:p.Ser445=
XM_011517849.2:c.1582-101T=	XP_011516151.1:n.1582-101T=
XM_017014625.2:c.1321T=	XP_016870114.1:p.Ser441=
XR_002956774.1:n.1783-101T=
XR_929232.2:n.1783-101T=
XR_929233.2:n.1783-101T=
NM_012144.4:c.1579T= MANE Select	NP_036276.1:p.Ser527=
NM_001281428.2:c.1591T=	NP_001268357.1:p.Ser531=