Canonical Allele Identifier: CA373266324

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517305T>G (hg19) ; chr9:g.34517307T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517307T>G , CM000671.2:g.34517307T>G	GRCh38
NC_000009.11:g.34517305T>G , CM000671.1:g.34517305T>G	GRCh37
NC_000009.10:g.34507305T>G	NCBI36
NG_008127.1:g.63495T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1841T>G MANE Select	ENSP00000242317.4:p.Ile614Ser
ENST00000242317.8:c.1841T>G	ENSP00000242317.4:p.Ile614Ser
ENST00000442556.1:c.329+2568T>G
ENST00000470169.5:c.629T>G
ENST00000485580.1:n.417T>G
ENST00000614641.4:c.1853T>G	ENSP00000480538.1:p.Ile618Ser
NM_001281428.1:c.1853T>G	NP_001268357.1:p.Ile618Ser
NM_012144.3:c.1841T>G	NP_036276.1:p.Ile614Ser
XM_006716758.2:c.1310T>G	XP_006716821.1:p.Ile437Ser
XM_011517848.1:c.1595T>G	XP_011516150.1:p.Ile532Ser
XM_006716758.3:c.1310T>G	XP_006716821.1:p.Ile437Ser
XM_011517848.2:c.1595T>G	XP_011516150.1:p.Ile532Ser
XM_017014625.2:c.1583T>G	XP_016870114.1:p.Ile528Ser
XR_002956774.1:n.1944T>G
NM_012144.4:c.1841T>G MANE Select	NP_036276.1:p.Ile614Ser
NM_001281428.2:c.1853T>G	NP_001268357.1:p.Ile618Ser