Canonical Allele Identifier: CA2739269217

Gene: DNAI1

Linked Data

• ClinVar Variation Id: 2778721
• ClinVar RCV Id: RCV003648059

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34489310C>T , CM000671.2:g.34489310C>T	GRCh38
NC_000009.11:g.34489308C>T , CM000671.1:g.34489308C>T	GRCh37
NC_000009.10:g.34479308C>T	NCBI36
NG_008127.1:g.35498C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.262-13C>T MANE Select	ENSP00000242317.4:n.262-13C>T
ENST00000242317.8:c.262-13C>T	ENSP00000242317.4:n.262-13C>T
ENST00000437363.5:c.229-13C>T	ENSP00000395396.1:n.229-13C>T
ENST00000488369.1:n.378-13C>T
ENST00000614641.4:c.262-13C>T	ENSP00000480538.1:n.262-13C>T
NM_001281428.1:c.262-13C>T	NP_001268357.1:n.262-13C>T
NM_012144.3:c.262-13C>T	NP_036276.1:n.262-13C>T
XM_011517846.1:c.262-13C>T	XP_011516148.1:n.262-13C>T
XM_011517847.1:c.262-13C>T	XP_011516149.1:n.262-13C>T
XM_011517848.1:c.262-13C>T	XP_011516150.1:n.262-13C>T
XM_011517849.1:c.262-13C>T	XP_011516151.1:n.262-13C>T
XM_011517850.1:c.262-13C>T	XP_011516152.1:n.262-13C>T
XR_929232.1:n.516-13C>T
XR_929233.1:n.516-13C>T
XR_929235.1:n.516-13C>T
XM_006716758.3:c.-215-13C>T	XP_006716821.1:n.-215-13C>T
XM_011517846.2:c.262-13C>T	XP_011516148.1:n.262-13C>T
XM_011517847.3:c.262-13C>T	XP_011516149.1:n.262-13C>T
XM_011517848.2:c.262-13C>T	XP_011516150.1:n.262-13C>T
XM_011517849.2:c.262-13C>T	XP_011516151.1:n.262-13C>T
XM_011517850.3:c.262-13C>T	XP_011516152.1:n.262-13C>T
XM_017014625.2:c.262-13C>T	XP_016870114.1:n.262-13C>T
XR_002956774.1:n.463-13C>T
XR_929232.2:n.463-13C>T
XR_929233.2:n.463-13C>T
NM_012144.4:c.262-13C>T MANE Select	NP_036276.1:n.262-13C>T
NM_001281428.2:c.262-13C>T	NP_001268357.1:n.262-13C>T