Canonical Allele Identifier: CA1845590958

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517073_34517074delinsAT , CM000671.2:g.34517073_34517074delinsAT	GRCh38
NC_000009.11:g.34517071_34517072delinsAT , CM000671.1:g.34517071_34517072delinsAT	GRCh37
NC_000009.10:g.34507071_34507072delinsAT	NCBI36
NG_008127.1:g.63261_63262delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-212_1819-211delinsAT MANE Select	ENSP00000242317.4:n.1819-212_1819-211delinsAT
ENST00000242317.8:c.1819-212_1819-211delinsAT	ENSP00000242317.4:n.1819-212_1819-211delinsAT
ENST00000442556.1:c.329+2334_329+2335delinsAT
ENST00000470169.5:c.607-212_607-211delinsAT
ENST00000485580.1:n.395-212_395-211delinsAT
ENST00000614641.4:c.1831-212_1831-211delinsAT	ENSP00000480538.1:n.1831-212_1831-211delinsAT
NM_001281428.1:c.1831-212_1831-211delinsAT	NP_001268357.1:n.1831-212_1831-211delinsAT
NM_012144.3:c.1819-212_1819-211delinsAT	NP_036276.1:n.1819-212_1819-211delinsAT
XM_006716758.2:c.1288-212_1288-211delinsAT	XP_006716821.1:n.1288-212_1288-211delinsAT
XM_011517847.1:c.1831-122_1831-121delinsAT	XP_011516149.1:n.1831-122_1831-121delinsAT
XM_011517848.1:c.1573-212_1573-211delinsAT	XP_011516150.1:n.1573-212_1573-211delinsAT
XR_929233.1:n.1975-122_1975-121delinsAT
XM_006716758.3:c.1288-212_1288-211delinsAT	XP_006716821.1:n.1288-212_1288-211delinsAT
XM_011517847.3:c.1831-122_1831-121delinsAT	XP_011516149.1:n.1831-122_1831-121delinsAT
XM_011517848.2:c.1573-212_1573-211delinsAT	XP_011516150.1:n.1573-212_1573-211delinsAT
XM_017014625.2:c.1561-212_1561-211delinsAT	XP_016870114.1:n.1561-212_1561-211delinsAT
XR_002956774.1:n.1922-212_1922-211delinsAT
XR_929233.2:n.1922-122_1922-121delinsAT
NM_012144.4:c.1819-212_1819-211delinsAT MANE Select	NP_036276.1:n.1819-212_1819-211delinsAT
NM_001281428.2:c.1831-212_1831-211delinsAT	NP_001268357.1:n.1831-212_1831-211delinsAT