Canonical Allele Identifier: CA863462662

Gene: DNAI1

Linked Data

• dbSNP Id: rs1425020976
• MyVariant Identifiers: chr9:g.34517246A>C (hg19) ; chr9:g.34517248A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517248A>C , CM000671.2:g.34517248A>C	GRCh38
NC_000009.11:g.34517246A>C , CM000671.1:g.34517246A>C	GRCh37
NC_000009.10:g.34507246A>C	NCBI36
NG_008127.1:g.63436A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-37A>C MANE Select	ENSP00000242317.4:n.1819-37A>C
ENST00000242317.8:c.1819-37A>C	ENSP00000242317.4:n.1819-37A>C
ENST00000442556.1:c.329+2509A>C
ENST00000470169.5:c.607-37A>C
ENST00000485580.1:n.395-37A>C
ENST00000614641.4:c.1831-37A>C	ENSP00000480538.1:n.1831-37A>C
NM_001281428.1:c.1831-37A>C	NP_001268357.1:n.1831-37A>C
NM_012144.3:c.1819-37A>C	NP_036276.1:n.1819-37A>C
XM_006716758.2:c.1288-37A>C	XP_006716821.1:n.1288-37A>C
XM_011517847.1:c.*18A>C	XP_011516149.1:n.*18A>C
XM_011517848.1:c.1573-37A>C	XP_011516150.1:n.1573-37A>C
XR_929233.1:n.2028A>C
XM_006716758.3:c.1288-37A>C	XP_006716821.1:n.1288-37A>C
XM_011517847.3:c.*18A>C	XP_011516149.1:n.*18A>C
XM_011517848.2:c.1573-37A>C	XP_011516150.1:n.1573-37A>C
XM_017014625.2:c.1561-37A>C	XP_016870114.1:n.1561-37A>C
XR_002956774.1:n.1922-37A>C
XR_929233.2:n.1975A>C
NM_012144.4:c.1819-37A>C MANE Select	NP_036276.1:n.1819-37A>C
NM_001281428.2:c.1831-37A>C	NP_001268357.1:n.1831-37A>C