Canonical Allele Identifier: CA373267122

Gene: DNAI1

Linked Data

• MyVariant Identifiers: chr9:g.34517467T>C (hg19) ; chr9:g.34517469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517469T>C , CM000671.2:g.34517469T>C	GRCh38
NC_000009.11:g.34517467T>C , CM000671.1:g.34517467T>C	GRCh37
NC_000009.10:g.34507467T>C	NCBI36
NG_008127.1:g.63657T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000242317.9:c.2001+2T>C MANE Select	ENSP00000242317.4:n.2001+2T>C
ENST00000242317.8:c.2001+2T>C	ENSP00000242317.4:n.2001+2T>C
ENST00000442556.1:c.329+2730T>C
ENST00000614641.4:c.2013+2T>C	ENSP00000480538.1:n.2013+2T>C
NM_001281428.1:c.2013+2T>C	NP_001268357.1:n.2013+2T>C
NM_012144.3:c.2001+2T>C	NP_036276.1:n.2001+2T>C
XM_006716758.2:c.1470+2T>C	XP_006716821.1:n.1470+2T>C
XM_011517848.1:c.1755+2T>C	XP_011516150.1:n.1755+2T>C
XM_006716758.3:c.1470+2T>C	XP_006716821.1:n.1470+2T>C
XM_011517848.2:c.1755+2T>C	XP_011516150.1:n.1755+2T>C
XM_017014625.2:c.1743+2T>C	XP_016870114.1:n.1743+2T>C
XR_002956774.1:n.2104+2T>C
NM_012144.4:c.2001+2T>C MANE Select	NP_036276.1:n.2001+2T>C
NM_001281428.2:c.2013+2T>C	NP_001268357.1:n.2013+2T>C