Canonical Allele Identifier: CA373266542

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517329A>T (hg19) ; chr9:g.34517331A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517331A>T , CM000671.2:g.34517331A>T	GRCh38
NC_000009.11:g.34517329A>T , CM000671.1:g.34517329A>T	GRCh37
NC_000009.10:g.34507329A>T	NCBI36
NG_008127.1:g.63519A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1865A>T MANE Select	ENSP00000242317.4:p.Asn622Ile
ENST00000242317.8:c.1865A>T	ENSP00000242317.4:p.Asn622Ile
ENST00000442556.1:c.329+2592A>T
ENST00000470169.5:c.653A>T
ENST00000485580.1:n.441A>T
ENST00000614641.4:c.1877A>T	ENSP00000480538.1:p.Asn626Ile
NM_001281428.1:c.1877A>T	NP_001268357.1:p.Asn626Ile
NM_012144.3:c.1865A>T	NP_036276.1:p.Asn622Ile
XM_006716758.2:c.1334A>T	XP_006716821.1:p.Asn445Ile
XM_011517848.1:c.1619A>T	XP_011516150.1:p.Asn540Ile
XM_006716758.3:c.1334A>T	XP_006716821.1:p.Asn445Ile
XM_011517848.2:c.1619A>T	XP_011516150.1:p.Asn540Ile
XM_017014625.2:c.1607A>T	XP_016870114.1:p.Asn536Ile
XR_002956774.1:n.1968A>T
NM_012144.4:c.1865A>T MANE Select	NP_036276.1:p.Asn622Ile
NM_001281428.2:c.1877A>T	NP_001268357.1:p.Asn626Ile