Canonical Allele Identifier: CA1845592553

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517501C= , CM000671.2:g.34517501C=	GRCh38
NC_000009.11:g.34517499C= , CM000671.1:g.34517499C=	GRCh37
NC_000009.10:g.34507499C=	NCBI36
NG_008127.1:g.63689C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000242317.9:c.2001+34C= MANE Select	ENSP00000242317.4:n.2001+34C=
ENST00000242317.8:c.2001+34C=	ENSP00000242317.4:n.2001+34C=
ENST00000442556.1:c.329+2762C=
ENST00000614641.4:c.2013+34C=	ENSP00000480538.1:n.2013+34C=
NM_001281428.1:c.2013+34C=	NP_001268357.1:n.2013+34C=
NM_012144.3:c.2001+34C=	NP_036276.1:n.2001+34C=
XM_006716758.2:c.1470+34C=	XP_006716821.1:n.1470+34C=
XM_011517848.1:c.1755+34C=	XP_011516150.1:n.1755+34C=
XM_006716758.3:c.1470+34C=	XP_006716821.1:n.1470+34C=
XM_011517848.2:c.1755+34C=	XP_011516150.1:n.1755+34C=
XM_017014625.2:c.1743+34C=	XP_016870114.1:n.1743+34C=
XR_002956774.1:n.2104+34C=
NM_012144.4:c.2001+34C= MANE Select	NP_036276.1:n.2001+34C=
NM_001281428.2:c.2013+34C=	NP_001268357.1:n.2013+34C=