Canonical Allele Identifier: CA1845574578

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34489313_34489316delinsCTCT , CM000671.2:g.34489313_34489316delinsCTCT	GRCh38
NC_000009.11:g.34489311_34489314delinsCTCT , CM000671.1:g.34489311_34489314delinsCTCT	GRCh37
NC_000009.10:g.34479311_34479314delinsCTCT	NCBI36
NG_008127.1:g.35501_35504delinsCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.262-10_262-7delinsCTCT MANE Select	ENSP00000242317.4:n.262-10_262-7delinsCTCT
ENST00000242317.8:c.262-10_262-7delinsCTCT	ENSP00000242317.4:n.262-10_262-7delinsCTCT
ENST00000437363.5:c.229-10_229-7delinsCTCT	ENSP00000395396.1:n.229-10_229-7delinsCTCT
ENST00000488369.1:n.378-10_378-7delinsCTCT
ENST00000614641.4:c.262-10_262-7delinsCTCT	ENSP00000480538.1:n.262-10_262-7delinsCTCT
NM_001281428.1:c.262-10_262-7delinsCTCT	NP_001268357.1:n.262-10_262-7delinsCTCT
NM_012144.3:c.262-10_262-7delinsCTCT	NP_036276.1:n.262-10_262-7delinsCTCT
XM_011517846.1:c.262-10_262-7delinsCTCT	XP_011516148.1:n.262-10_262-7delinsCTCT
XM_011517847.1:c.262-10_262-7delinsCTCT	XP_011516149.1:n.262-10_262-7delinsCTCT
XM_011517848.1:c.262-10_262-7delinsCTCT	XP_011516150.1:n.262-10_262-7delinsCTCT
XM_011517849.1:c.262-10_262-7delinsCTCT	XP_011516151.1:n.262-10_262-7delinsCTCT
XM_011517850.1:c.262-10_262-7delinsCTCT	XP_011516152.1:n.262-10_262-7delinsCTCT
XR_929232.1:n.516-10_516-7delinsCTCT
XR_929233.1:n.516-10_516-7delinsCTCT
XR_929235.1:n.516-10_516-7delinsCTCT
XM_006716758.3:c.-215-10_-215-7delinsCTCT	XP_006716821.1:n.-215-10_-215-7delinsCTCT
XM_011517846.2:c.262-10_262-7delinsCTCT	XP_011516148.1:n.262-10_262-7delinsCTCT
XM_011517847.3:c.262-10_262-7delinsCTCT	XP_011516149.1:n.262-10_262-7delinsCTCT
XM_011517848.2:c.262-10_262-7delinsCTCT	XP_011516150.1:n.262-10_262-7delinsCTCT
XM_011517849.2:c.262-10_262-7delinsCTCT	XP_011516151.1:n.262-10_262-7delinsCTCT
XM_011517850.3:c.262-10_262-7delinsCTCT	XP_011516152.1:n.262-10_262-7delinsCTCT
XM_017014625.2:c.262-10_262-7delinsCTCT	XP_016870114.1:n.262-10_262-7delinsCTCT
XR_002956774.1:n.463-10_463-7delinsCTCT
XR_929232.2:n.463-10_463-7delinsCTCT
XR_929233.2:n.463-10_463-7delinsCTCT
NM_012144.4:c.262-10_262-7delinsCTCT MANE Select	NP_036276.1:n.262-10_262-7delinsCTCT
NM_001281428.2:c.262-10_262-7delinsCTCT	NP_001268357.1:n.262-10_262-7delinsCTCT