Canonical Allele Identifier: CA464398333

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517306C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517308C>A , CM000671.2:g.34517308C>A	GRCh38
NC_000009.11:g.34517306C>A , CM000671.1:g.34517306C>A	GRCh37
NC_000009.10:g.34507306C>A	NCBI36
NG_008127.1:g.63496C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1842C>A MANE Select	ENSP00000242317.4:p.Ile614=
ENST00000242317.8:c.1842C>A	ENSP00000242317.4:p.Ile614=
ENST00000442556.1:c.329+2569C>A
ENST00000470169.5:c.630C>A
ENST00000485580.1:n.418C>A
ENST00000614641.4:c.1854C>A	ENSP00000480538.1:p.Ile618=
NM_001281428.1:c.1854C>A	NP_001268357.1:p.Ile618=
NM_012144.3:c.1842C>A	NP_036276.1:p.Ile614=
XM_006716758.2:c.1311C>A	XP_006716821.1:p.Ile437=
XM_011517848.1:c.1596C>A	XP_011516150.1:p.Ile532=
XM_006716758.3:c.1311C>A	XP_006716821.1:p.Ile437=
XM_011517848.2:c.1596C>A	XP_011516150.1:p.Ile532=
XM_017014625.2:c.1584C>A	XP_016870114.1:p.Ile528=
XR_002956774.1:n.1945C>A
NM_012144.4:c.1842C>A MANE Select	NP_036276.1:p.Ile614=
NM_001281428.2:c.1854C>A	NP_001268357.1:p.Ile618=