Canonical Allele Identifier: CA464398336

Gene: DNAI1

Linked Data

• dbSNP Id: rs1825187906
• MyVariant Identifiers: chr9:g.34517315T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517317T>C , CM000671.2:g.34517317T>C	GRCh38
NC_000009.11:g.34517315T>C , CM000671.1:g.34517315T>C	GRCh37
NC_000009.10:g.34507315T>C	NCBI36
NG_008127.1:g.63505T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1851T>C MANE Select	ENSP00000242317.4:p.Tyr617=
ENST00000242317.8:c.1851T>C	ENSP00000242317.4:p.Tyr617=
ENST00000442556.1:c.329+2578T>C
ENST00000470169.5:c.639T>C
ENST00000485580.1:n.427T>C
ENST00000614641.4:c.1863T>C	ENSP00000480538.1:p.Tyr621=
NM_001281428.1:c.1863T>C	NP_001268357.1:p.Tyr621=
NM_012144.3:c.1851T>C	NP_036276.1:p.Tyr617=
XM_006716758.2:c.1320T>C	XP_006716821.1:p.Tyr440=
XM_011517848.1:c.1605T>C	XP_011516150.1:p.Tyr535=
XM_006716758.3:c.1320T>C	XP_006716821.1:p.Tyr440=
XM_011517848.2:c.1605T>C	XP_011516150.1:p.Tyr535=
XM_017014625.2:c.1593T>C	XP_016870114.1:p.Tyr531=
XR_002956774.1:n.1954T>C
NM_012144.4:c.1851T>C MANE Select	NP_036276.1:p.Tyr617=
NM_001281428.2:c.1863T>C	NP_001268357.1:p.Tyr621=