Canonical Allele Identifier: CA373266209

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517292T>A (hg19) ; chr9:g.34517294T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517294T>A , CM000671.2:g.34517294T>A	GRCh38
NC_000009.11:g.34517292T>A , CM000671.1:g.34517292T>A	GRCh37
NC_000009.10:g.34507292T>A	NCBI36
NG_008127.1:g.63482T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1828T>A MANE Select	ENSP00000242317.4:p.Phe610Ile
ENST00000242317.8:c.1828T>A	ENSP00000242317.4:p.Phe610Ile
ENST00000442556.1:c.329+2555T>A
ENST00000470169.5:c.616T>A
ENST00000485580.1:n.404T>A
ENST00000614641.4:c.1840T>A	ENSP00000480538.1:p.Phe614Ile
NM_001281428.1:c.1840T>A	NP_001268357.1:p.Phe614Ile
NM_012144.3:c.1828T>A	NP_036276.1:p.Phe610Ile
XM_006716758.2:c.1297T>A	XP_006716821.1:p.Phe433Ile
XM_011517848.1:c.1582T>A	XP_011516150.1:p.Phe528Ile
XM_006716758.3:c.1297T>A	XP_006716821.1:p.Phe433Ile
XM_011517848.2:c.1582T>A	XP_011516150.1:p.Phe528Ile
XM_017014625.2:c.1570T>A	XP_016870114.1:p.Phe524Ile
XR_002956774.1:n.1931T>A
NM_012144.4:c.1828T>A MANE Select	NP_036276.1:p.Phe610Ile
NM_001281428.2:c.1840T>A	NP_001268357.1:p.Phe614Ile