Canonical Allele Identifier: CA5034372

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34512201G>A , CM000671.2:g.34512201G>A	GRCh38
NC_000009.11:g.34512199G>A , CM000671.1:g.34512199G>A	GRCh37
NC_000009.10:g.34502199G>A	NCBI36
NG_008127.1:g.58389G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012144.4:c.1401+3G>A MANE Select	NP_036276.1:n.1401+3G>A
ENST00000242317.9:c.1401+3G>A MANE Select	ENSP00000242317.4:n.1401+3G>A
NM_001281428.1:c.1413+3G>A	NP_001268357.1:n.1413+3G>A
NM_001281428.2:c.1413+3G>A	NP_001268357.1:n.1413+3G>A
NM_012144.3:c.1401+3G>A	NP_036276.1:n.1401+3G>A
ENST00000242317.8:c.1401+3G>A	ENSP00000242317.4:n.1401+3G>A
ENST00000470169.5:c.338+3G>A
ENST00000614641.4:c.1413+3G>A	ENSP00000480538.1:n.1413+3G>A
XM_006716758.2:c.870+3G>A	XP_006716821.1:n.870+3G>A
XM_006716758.3:c.870+3G>A	XP_006716821.1:n.870+3G>A
XM_011517846.1:c.1413+3G>A	XP_011516148.1:n.1413+3G>A
XM_011517846.2:c.1413+3G>A	XP_011516148.1:n.1413+3G>A
XM_011517847.1:c.1413+3G>A	XP_011516149.1:n.1413+3G>A
XM_011517847.3:c.1413+3G>A	XP_011516149.1:n.1413+3G>A
XM_011517848.1:c.1324-2193G>A	XP_011516150.1:n.1324-2193G>A
XM_011517848.2:c.1324-2193G>A	XP_011516150.1:n.1324-2193G>A
XM_011517849.1:c.1413+3G>A	XP_011516151.1:n.1413+3G>A
XM_011517849.2:c.1413+3G>A	XP_011516151.1:n.1413+3G>A
XM_017014625.2:c.1312-2193G>A	XP_016870114.1:n.1312-2193G>A
XR_002956774.1:n.1614+3G>A
XR_929232.1:n.1667+3G>A
XR_929232.2:n.1614+3G>A
XR_929233.1:n.1667+3G>A
XR_929233.2:n.1614+3G>A
XR_929235.1:n.1578-2303G>A