Canonical Allele Identifier: CA373266552

Gene: DNAI1

Linked Data

• gnomAD v4: 9-34517334-A-C
• MyVariant Identifiers: chr9:g.34517332A>C (hg19) ; chr9:g.34517334A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517334A>C , CM000671.2:g.34517334A>C	GRCh38
NC_000009.11:g.34517332A>C , CM000671.1:g.34517332A>C	GRCh37
NC_000009.10:g.34507332A>C	NCBI36
NG_008127.1:g.63522A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1868A>C MANE Select	ENSP00000242317.4:p.Gln623Pro
ENST00000242317.8:c.1868A>C	ENSP00000242317.4:p.Gln623Pro
ENST00000442556.1:c.329+2595A>C
ENST00000470169.5:c.656A>C
ENST00000485580.1:n.444A>C
ENST00000614641.4:c.1880A>C	ENSP00000480538.1:p.Gln627Pro
NM_001281428.1:c.1880A>C	NP_001268357.1:p.Gln627Pro
NM_012144.3:c.1868A>C	NP_036276.1:p.Gln623Pro
XM_006716758.2:c.1337A>C	XP_006716821.1:p.Gln446Pro
XM_011517848.1:c.1622A>C	XP_011516150.1:p.Gln541Pro
XM_006716758.3:c.1337A>C	XP_006716821.1:p.Gln446Pro
XM_011517848.2:c.1622A>C	XP_011516150.1:p.Gln541Pro
XM_017014625.2:c.1610A>C	XP_016870114.1:p.Gln537Pro
XR_002956774.1:n.1971A>C
NM_012144.4:c.1868A>C MANE Select	NP_036276.1:p.Gln623Pro
NM_001281428.2:c.1880A>C	NP_001268357.1:p.Gln627Pro