Canonical Allele Identifier: CA1845592581

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517502G= , CM000671.2:g.34517502G=	GRCh38
NC_000009.11:g.34517500G= , CM000671.1:g.34517500G=	GRCh37
NC_000009.10:g.34507500G=	NCBI36
NG_008127.1:g.63690G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000242317.9:c.2001+35G= MANE Select	ENSP00000242317.4:n.2001+35G=
ENST00000242317.8:c.2001+35G=	ENSP00000242317.4:n.2001+35G=
ENST00000442556.1:c.329+2763G=
ENST00000614641.4:c.2013+35G=	ENSP00000480538.1:n.2013+35G=
NM_001281428.1:c.2013+35G=	NP_001268357.1:n.2013+35G=
NM_012144.3:c.2001+35G=	NP_036276.1:n.2001+35G=
XM_006716758.2:c.1470+35G=	XP_006716821.1:n.1470+35G=
XM_011517848.1:c.1755+35G=	XP_011516150.1:n.1755+35G=
XM_006716758.3:c.1470+35G=	XP_006716821.1:n.1470+35G=
XM_011517848.2:c.1755+35G=	XP_011516150.1:n.1755+35G=
XM_017014625.2:c.1743+35G=	XP_016870114.1:n.1743+35G=
XR_002956774.1:n.2104+35G=
NM_012144.4:c.2001+35G= MANE Select	NP_036276.1:n.2001+35G=
NM_001281428.2:c.2013+35G=	NP_001268357.1:n.2013+35G=