Canonical Allele Identifier: CA373266215

Gene: DNAI1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1828T>G MANE Select	ENSP00000242317.4:p.Phe610Val
ENST00000242317.8:c.1828T>G	ENSP00000242317.4:p.Phe610Val
ENST00000442556.1:c.329+2555T>G
ENST00000470169.5:c.616T>G
ENST00000485580.1:n.404T>G
ENST00000614641.4:c.1840T>G	ENSP00000480538.1:p.Phe614Val
NM_001281428.1:c.1840T>G	NP_001268357.1:p.Phe614Val
NM_012144.3:c.1828T>G	NP_036276.1:p.Phe610Val
XM_006716758.2:c.1297T>G	XP_006716821.1:p.Phe433Val
XM_011517848.1:c.1582T>G	XP_011516150.1:p.Phe528Val
XM_006716758.3:c.1297T>G	XP_006716821.1:p.Phe433Val
XM_011517848.2:c.1582T>G	XP_011516150.1:p.Phe528Val
XM_017014625.2:c.1570T>G	XP_016870114.1:p.Phe524Val
XR_002956774.1:n.1931T>G
NM_012144.4:c.1828T>G MANE Select	NP_036276.1:p.Phe610Val
NM_001281428.2:c.1840T>G	NP_001268357.1:p.Phe614Val