Canonical Allele Identifier: CA1845591897

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517373A= , CM000671.2:g.34517373A=	GRCh38
NC_000009.11:g.34517371A= , CM000671.1:g.34517371A=	GRCh37
NC_000009.10:g.34507371A=	NCBI36
NG_008127.1:g.63561A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1907A= MANE Select	ENSP00000242317.4:p.Gln636=
ENST00000242317.8:c.1907A=	ENSP00000242317.4:p.Gln636=
ENST00000442556.1:c.329+2634A=
ENST00000470169.5:c.695A=
ENST00000485580.1:n.483A=
ENST00000614641.4:c.1919A=	ENSP00000480538.1:p.Gln640=
NM_001281428.1:c.1919A=	NP_001268357.1:p.Gln640=
NM_012144.3:c.1907A=	NP_036276.1:p.Gln636=
XM_006716758.2:c.1376A=	XP_006716821.1:p.Gln459=
XM_011517848.1:c.1661A=	XP_011516150.1:p.Gln554=
XM_006716758.3:c.1376A=	XP_006716821.1:p.Gln459=
XM_011517848.2:c.1661A=	XP_011516150.1:p.Gln554=
XM_017014625.2:c.1649A=	XP_016870114.1:p.Gln550=
XR_002956774.1:n.2010A=
NM_012144.4:c.1907A= MANE Select	NP_036276.1:p.Gln636=
NM_001281428.2:c.1919A=	NP_001268357.1:p.Gln640=