Canonical Allele Identifier: CA1845591644

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517335_34517336delinsGC , CM000671.2:g.34517335_34517336delinsGC	GRCh38
NC_000009.11:g.34517333_34517334delinsGC , CM000671.1:g.34517333_34517334delinsGC	GRCh37
NC_000009.10:g.34507333_34507334delinsGC	NCBI36
NG_008127.1:g.63523_63524delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1869_1870delinsGC MANE Select	ENSP00000242317.4:p.Gln623=
ENST00000242317.8:c.1869_1870delinsGC	ENSP00000242317.4:p.Gln623=
ENST00000442556.1:c.329+2596_329+2597delinsGC
ENST00000470169.5:c.657_658delinsGC
ENST00000485580.1:n.445_446delinsGC
ENST00000614641.4:c.1881_1882delinsGC	ENSP00000480538.1:p.Gln627=
NM_001281428.1:c.1881_1882delinsGC	NP_001268357.1:p.Gln627=
NM_012144.3:c.1869_1870delinsGC	NP_036276.1:p.Gln623=
XM_006716758.2:c.1338_1339delinsGC	XP_006716821.1:p.Gln446=
XM_011517848.1:c.1623_1624delinsGC	XP_011516150.1:p.Gln541=
XM_006716758.3:c.1338_1339delinsGC	XP_006716821.1:p.Gln446=
XM_011517848.2:c.1623_1624delinsGC	XP_011516150.1:p.Gln541=
XM_017014625.2:c.1611_1612delinsGC	XP_016870114.1:p.Gln537=
XR_002956774.1:n.1972_1973delinsGC
NM_012144.4:c.1869_1870delinsGC MANE Select	NP_036276.1:p.Gln623=
NM_001281428.2:c.1881_1882delinsGC	NP_001268357.1:p.Gln627=