Canonical Allele Identifier: CA1845610213

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514352G= , CM000671.2:g.34514352G=	GRCh38
NC_000009.11:g.34514350G= , CM000671.1:g.34514350G=	GRCh37
NC_000009.10:g.34504350G=	NCBI36
NG_008127.1:g.60540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1570-42G= MANE Select	ENSP00000242317.4:n.1570-42G=
ENST00000242317.8:c.1570-42G=	ENSP00000242317.4:n.1570-42G=
ENST00000442556.1:c.81-42G=
ENST00000470169.5:c.507-288G=
ENST00000485580.1:n.49-42G=
ENST00000614641.4:c.1582-42G=	ENSP00000480538.1:n.1582-42G=
NM_001281428.1:c.1582-42G=	NP_001268357.1:n.1582-42G=
NM_012144.3:c.1570-42G=	NP_036276.1:n.1570-42G=
XM_006716758.2:c.1039-42G=	XP_006716821.1:n.1039-42G=
XM_011517846.1:c.1582-42G=	XP_011516148.1:n.1582-42G=
XM_011517847.1:c.1582-42G=	XP_011516149.1:n.1582-42G=
XM_011517848.1:c.1324-42G=	XP_011516150.1:n.1324-42G=
XM_011517849.1:c.1582-152G=	XP_011516151.1:n.1582-152G=
XR_929232.1:n.1836-152G=
XR_929233.1:n.1836-152G=
XR_929235.1:n.1578-152G=
XM_006716758.3:c.1039-42G=	XP_006716821.1:n.1039-42G=
XM_011517846.2:c.1582-42G=	XP_011516148.1:n.1582-42G=
XM_011517847.3:c.1582-42G=	XP_011516149.1:n.1582-42G=
XM_011517848.2:c.1324-42G=	XP_011516150.1:n.1324-42G=
XM_011517849.2:c.1582-152G=	XP_011516151.1:n.1582-152G=
XM_017014625.2:c.1312-42G=	XP_016870114.1:n.1312-42G=
XR_002956774.1:n.1783-152G=
XR_929232.2:n.1783-152G=
XR_929233.2:n.1783-152G=
NM_012144.4:c.1570-42G= MANE Select	NP_036276.1:n.1570-42G=
NM_001281428.2:c.1582-42G=	NP_001268357.1:n.1582-42G=