Canonical Allele Identifier: CA464398365

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517369G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517371G>C , CM000671.2:g.34517371G>C	GRCh38
NC_000009.11:g.34517369G>C , CM000671.1:g.34517369G>C	GRCh37
NC_000009.10:g.34507369G>C	NCBI36
NG_008127.1:g.63559G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1905G>C MANE Select	ENSP00000242317.4:p.Val635=
ENST00000242317.8:c.1905G>C	ENSP00000242317.4:p.Val635=
ENST00000442556.1:c.329+2632G>C
ENST00000470169.5:c.693G>C
ENST00000485580.1:n.481G>C
ENST00000614641.4:c.1917G>C	ENSP00000480538.1:p.Val639=
NM_001281428.1:c.1917G>C	NP_001268357.1:p.Val639=
NM_012144.3:c.1905G>C	NP_036276.1:p.Val635=
XM_006716758.2:c.1374G>C	XP_006716821.1:p.Val458=
XM_011517848.1:c.1659G>C	XP_011516150.1:p.Val553=
XM_006716758.3:c.1374G>C	XP_006716821.1:p.Val458=
XM_011517848.2:c.1659G>C	XP_011516150.1:p.Val553=
XM_017014625.2:c.1647G>C	XP_016870114.1:p.Val549=
XR_002956774.1:n.2008G>C
NM_012144.4:c.1905G>C MANE Select	NP_036276.1:p.Val635=
NM_001281428.2:c.1917G>C	NP_001268357.1:p.Val639=