Canonical Allele Identifier: CA373263126

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34514413C>A (hg19) ; chr9:g.34514415C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514415C>A , CM000671.2:g.34514415C>A	GRCh38
NC_000009.11:g.34514413C>A , CM000671.1:g.34514413C>A	GRCh37
NC_000009.10:g.34504413C>A	NCBI36
NG_008127.1:g.60603C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1591C>A MANE Select	ENSP00000242317.4:p.Gln531Lys
ENST00000242317.8:c.1591C>A	ENSP00000242317.4:p.Gln531Lys
ENST00000442556.1:c.102C>A
ENST00000470169.5:c.507-225C>A
ENST00000485580.1:n.70C>A
ENST00000614641.4:c.1603C>A	ENSP00000480538.1:p.Gln535Lys
NM_001281428.1:c.1603C>A	NP_001268357.1:p.Gln535Lys
NM_012144.3:c.1591C>A	NP_036276.1:p.Gln531Lys
XM_006716758.2:c.1060C>A	XP_006716821.1:p.Gln354Lys
XM_011517846.1:c.1603C>A	XP_011516148.1:p.Gln535Lys
XM_011517847.1:c.1603C>A	XP_011516149.1:p.Gln535Lys
XM_011517848.1:c.1345C>A	XP_011516150.1:p.Gln449Lys
XM_011517849.1:c.1582-89C>A	XP_011516151.1:n.1582-89C>A
XR_929232.1:n.1836-89C>A
XR_929233.1:n.1836-89C>A
XR_929235.1:n.1578-89C>A
XM_006716758.3:c.1060C>A	XP_006716821.1:p.Gln354Lys
XM_011517846.2:c.1603C>A	XP_011516148.1:p.Gln535Lys
XM_011517847.3:c.1603C>A	XP_011516149.1:p.Gln535Lys
XM_011517848.2:c.1345C>A	XP_011516150.1:p.Gln449Lys
XM_011517849.2:c.1582-89C>A	XP_011516151.1:n.1582-89C>A
XM_017014625.2:c.1333C>A	XP_016870114.1:p.Gln445Lys
XR_002956774.1:n.1783-89C>A
XR_929232.2:n.1783-89C>A
XR_929233.2:n.1783-89C>A
NM_012144.4:c.1591C>A MANE Select	NP_036276.1:p.Gln531Lys
NM_001281428.2:c.1603C>A	NP_001268357.1:p.Gln535Lys