Canonical Allele Identifier: CA1845571140

Gene: DNAI1

Linked Data

• ClinVar Variation Id: 1533353
• ClinVar RCV Id: RCV002107200
• dbSNP Id: rs1824445018

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34485130G>A , CM000671.2:g.34485130G>A	GRCh38
NC_000009.11:g.34485128G>A , CM000671.1:g.34485128G>A	GRCh37
NC_000009.10:g.34475128G>A	NCBI36
NG_008127.1:g.31318G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000242317.9:c.82-12G>A MANE Select	ENSP00000242317.4:n.82-12G>A
ENST00000242317.8:c.82-12G>A	ENSP00000242317.4:n.82-12G>A
ENST00000437363.5:c.49-12G>A	ENSP00000395396.1:n.49-12G>A
ENST00000470982.5:n.81-12G>A
ENST00000488369.1:n.85G>A
ENST00000614641.4:c.82-12G>A	ENSP00000480538.1:n.82-12G>A
NM_001281428.1:c.82-12G>A	NP_001268357.1:n.82-12G>A
NM_012144.3:c.82-12G>A	NP_036276.1:n.82-12G>A
XM_011517846.1:c.82-12G>A	XP_011516148.1:n.82-12G>A
XM_011517847.1:c.82-12G>A	XP_011516149.1:n.82-12G>A
XM_011517848.1:c.82-12G>A	XP_011516150.1:n.82-12G>A
XM_011517849.1:c.82-12G>A	XP_011516151.1:n.82-12G>A
XM_011517850.1:c.82-12G>A	XP_011516152.1:n.82-12G>A
XR_929232.1:n.336-12G>A
XR_929233.1:n.336-12G>A
XR_929235.1:n.336-12G>A
XM_006716758.3:c.-395-12G>A	XP_006716821.1:n.-395-12G>A
XM_011517846.2:c.82-12G>A	XP_011516148.1:n.82-12G>A
XM_011517847.3:c.82-12G>A	XP_011516149.1:n.82-12G>A
XM_011517848.2:c.82-12G>A	XP_011516150.1:n.82-12G>A
XM_011517849.2:c.82-12G>A	XP_011516151.1:n.82-12G>A
XM_011517850.3:c.82-12G>A	XP_011516152.1:n.82-12G>A
XM_017014625.2:c.82-12G>A	XP_016870114.1:n.82-12G>A
XR_002956774.1:n.283-12G>A
XR_929232.2:n.283-12G>A
XR_929233.2:n.283-12G>A
NM_012144.4:c.82-12G>A MANE Select	NP_036276.1:n.82-12G>A
NM_001281428.2:c.82-12G>A	NP_001268357.1:n.82-12G>A