Canonical Allele Identifier: CA373266307

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517304A>T (hg19) ; chr9:g.34517306A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517306A>T , CM000671.2:g.34517306A>T	GRCh38
NC_000009.11:g.34517304A>T , CM000671.1:g.34517304A>T	GRCh37
NC_000009.10:g.34507304A>T	NCBI36
NG_008127.1:g.63494A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1840A>T MANE Select	ENSP00000242317.4:p.Ile614Phe
ENST00000242317.8:c.1840A>T	ENSP00000242317.4:p.Ile614Phe
ENST00000442556.1:c.329+2567A>T
ENST00000470169.5:c.628A>T
ENST00000485580.1:n.416A>T
ENST00000614641.4:c.1852A>T	ENSP00000480538.1:p.Ile618Phe
NM_001281428.1:c.1852A>T	NP_001268357.1:p.Ile618Phe
NM_012144.3:c.1840A>T	NP_036276.1:p.Ile614Phe
XM_006716758.2:c.1309A>T	XP_006716821.1:p.Ile437Phe
XM_011517848.1:c.1594A>T	XP_011516150.1:p.Ile532Phe
XM_006716758.3:c.1309A>T	XP_006716821.1:p.Ile437Phe
XM_011517848.2:c.1594A>T	XP_011516150.1:p.Ile532Phe
XM_017014625.2:c.1582A>T	XP_016870114.1:p.Ile528Phe
XR_002956774.1:n.1943A>T
NM_012144.4:c.1840A>T MANE Select	NP_036276.1:p.Ile614Phe
NM_001281428.2:c.1852A>T	NP_001268357.1:p.Ile618Phe