Canonical Allele Identifier: CA373263074

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34514406C>A (hg19) ; chr9:g.34514408C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514408C>A , CM000671.2:g.34514408C>A	GRCh38
NC_000009.11:g.34514406C>A , CM000671.1:g.34514406C>A	GRCh37
NC_000009.10:g.34504406C>A	NCBI36
NG_008127.1:g.60596C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1584C>A MANE Select	ENSP00000242317.4:p.Tyr528Ter
ENST00000242317.8:c.1584C>A	ENSP00000242317.4:p.Tyr528Ter
ENST00000442556.1:c.95C>A
ENST00000470169.5:c.507-232C>A
ENST00000485580.1:n.63C>A
ENST00000614641.4:c.1596C>A	ENSP00000480538.1:p.Tyr532Ter
NM_001281428.1:c.1596C>A	NP_001268357.1:p.Tyr532Ter
NM_012144.3:c.1584C>A	NP_036276.1:p.Tyr528Ter
XM_006716758.2:c.1053C>A	XP_006716821.1:p.Tyr351Ter
XM_011517846.1:c.1596C>A	XP_011516148.1:p.Tyr532Ter
XM_011517847.1:c.1596C>A	XP_011516149.1:p.Tyr532Ter
XM_011517848.1:c.1338C>A	XP_011516150.1:p.Tyr446Ter
XM_011517849.1:c.1582-96C>A	XP_011516151.1:n.1582-96C>A
XR_929232.1:n.1836-96C>A
XR_929233.1:n.1836-96C>A
XR_929235.1:n.1578-96C>A
XM_006716758.3:c.1053C>A	XP_006716821.1:p.Tyr351Ter
XM_011517846.2:c.1596C>A	XP_011516148.1:p.Tyr532Ter
XM_011517847.3:c.1596C>A	XP_011516149.1:p.Tyr532Ter
XM_011517848.2:c.1338C>A	XP_011516150.1:p.Tyr446Ter
XM_011517849.2:c.1582-96C>A	XP_011516151.1:n.1582-96C>A
XM_017014625.2:c.1326C>A	XP_016870114.1:p.Tyr442Ter
XR_002956774.1:n.1783-96C>A
XR_929232.2:n.1783-96C>A
XR_929233.2:n.1783-96C>A
NM_012144.4:c.1584C>A MANE Select	NP_036276.1:p.Tyr528Ter
NM_001281428.2:c.1596C>A	NP_001268357.1:p.Tyr532Ter