Canonical Allele Identifier: CA192653419

Gene: DNAI1

Linked Data

• dbSNP Id: rs756883156
• MyVariant Identifiers: chr9:g.34517247T>C (hg19) ; chr9:g.34517249T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517249T>C , CM000671.2:g.34517249T>C	GRCh38
NC_000009.11:g.34517247T>C , CM000671.1:g.34517247T>C	GRCh37
NC_000009.10:g.34507247T>C	NCBI36
NG_008127.1:g.63437T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-36T>C MANE Select	ENSP00000242317.4:n.1819-36T>C
ENST00000242317.8:c.1819-36T>C	ENSP00000242317.4:n.1819-36T>C
ENST00000442556.1:c.329+2510T>C
ENST00000470169.5:c.607-36T>C
ENST00000485580.1:n.395-36T>C
ENST00000614641.4:c.1831-36T>C	ENSP00000480538.1:n.1831-36T>C
NM_001281428.1:c.1831-36T>C	NP_001268357.1:n.1831-36T>C
NM_012144.3:c.1819-36T>C	NP_036276.1:n.1819-36T>C
XM_006716758.2:c.1288-36T>C	XP_006716821.1:n.1288-36T>C
XM_011517847.1:c.*19T>C	XP_011516149.1:n.*19T>C
XM_011517848.1:c.1573-36T>C	XP_011516150.1:n.1573-36T>C
XR_929233.1:n.2029T>C
XM_006716758.3:c.1288-36T>C	XP_006716821.1:n.1288-36T>C
XM_011517847.3:c.*19T>C	XP_011516149.1:n.*19T>C
XM_011517848.2:c.1573-36T>C	XP_011516150.1:n.1573-36T>C
XM_017014625.2:c.1561-36T>C	XP_016870114.1:n.1561-36T>C
XR_002956774.1:n.1922-36T>C
XR_929233.2:n.1976T>C
NM_012144.4:c.1819-36T>C MANE Select	NP_036276.1:n.1819-36T>C
NM_001281428.2:c.1831-36T>C	NP_001268357.1:n.1831-36T>C