Canonical Allele Identifier: CA1845591027

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517106_34517110delinsCTCTT , CM000671.2:g.34517106_34517110delinsCTCTT	GRCh38
NC_000009.11:g.34517104_34517108delinsCTCTT , CM000671.1:g.34517104_34517108delinsCTCTT	GRCh37
NC_000009.10:g.34507104_34507108delinsCTCTT	NCBI36
NG_008127.1:g.63294_63298delinsCTCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-179_1819-175delinsCTCTT MANE Select	ENSP00000242317.4:n.1819-179_1819-175delinsCTCTT
ENST00000242317.8:c.1819-179_1819-175delinsCTCTT	ENSP00000242317.4:n.1819-179_1819-175delinsCTCTT
ENST00000442556.1:c.329+2367_329+2371delinsCTCTT
ENST00000470169.5:c.607-179_607-175delinsCTCTT
ENST00000485580.1:n.395-179_395-175delinsCTCTT
ENST00000614641.4:c.1831-179_1831-175delinsCTCTT	ENSP00000480538.1:n.1831-179_1831-175delinsCTCTT
NM_001281428.1:c.1831-179_1831-175delinsCTCTT	NP_001268357.1:n.1831-179_1831-175delinsCTCTT
NM_012144.3:c.1819-179_1819-175delinsCTCTT	NP_036276.1:n.1819-179_1819-175delinsCTCTT
XM_006716758.2:c.1288-179_1288-175delinsCTCTT	XP_006716821.1:n.1288-179_1288-175delinsCTCTT
XM_011517847.1:c.1831-89_1831-85delinsCTCTT	XP_011516149.1:n.1831-89_1831-85delinsCTCTT
XM_011517848.1:c.1573-179_1573-175delinsCTCTT	XP_011516150.1:n.1573-179_1573-175delinsCTCTT
XR_929233.1:n.1975-89_1975-85delinsCTCTT
XM_006716758.3:c.1288-179_1288-175delinsCTCTT	XP_006716821.1:n.1288-179_1288-175delinsCTCTT
XM_011517847.3:c.1831-89_1831-85delinsCTCTT	XP_011516149.1:n.1831-89_1831-85delinsCTCTT
XM_011517848.2:c.1573-179_1573-175delinsCTCTT	XP_011516150.1:n.1573-179_1573-175delinsCTCTT
XM_017014625.2:c.1561-179_1561-175delinsCTCTT	XP_016870114.1:n.1561-179_1561-175delinsCTCTT
XR_002956774.1:n.1922-179_1922-175delinsCTCTT
XR_929233.2:n.1922-89_1922-85delinsCTCTT
NM_012144.4:c.1819-179_1819-175delinsCTCTT MANE Select	NP_036276.1:n.1819-179_1819-175delinsCTCTT
NM_001281428.2:c.1831-179_1831-175delinsCTCTT	NP_001268357.1:n.1831-179_1831-175delinsCTCTT