Canonical Allele Identifier: CA1845591805

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517356C= , CM000671.2:g.34517356C=	GRCh38
NC_000009.11:g.34517354C= , CM000671.1:g.34517354C=	GRCh37
NC_000009.10:g.34507354C=	NCBI36
NG_008127.1:g.63544C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1890C= MANE Select	ENSP00000242317.4:p.Asn630=
ENST00000242317.8:c.1890C=	ENSP00000242317.4:p.Asn630=
ENST00000442556.1:c.329+2617C=
ENST00000470169.5:c.678C=
ENST00000485580.1:n.466C=
ENST00000614641.4:c.1902C=	ENSP00000480538.1:p.Asn634=
NM_001281428.1:c.1902C=	NP_001268357.1:p.Asn634=
NM_012144.3:c.1890C=	NP_036276.1:p.Asn630=
XM_006716758.2:c.1359C=	XP_006716821.1:p.Asn453=
XM_011517848.1:c.1644C=	XP_011516150.1:p.Asn548=
XM_006716758.3:c.1359C=	XP_006716821.1:p.Asn453=
XM_011517848.2:c.1644C=	XP_011516150.1:p.Asn548=
XM_017014625.2:c.1632C=	XP_016870114.1:p.Asn544=
XR_002956774.1:n.1993C=
NM_012144.4:c.1890C= MANE Select	NP_036276.1:p.Asn630=
NM_001281428.2:c.1902C=	NP_001268357.1:p.Asn634=