Canonical Allele Identifier: CA863462619

Gene: DNAI1

Linked Data

• dbSNP Id: rs1239452432
• gnomAD v3: 9-34517125-AAC-A
• gnomAD v4: 9-34517125-AAC-A
• MyVariant Identifiers: chr9:g.34517124_34517125del (hg19) ; chr9:g.34517126_34517127del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517129_34517130del , CM000671.2:g.34517129_34517130del	GRCh38
NC_000009.11:g.34517127_34517128del , CM000671.1:g.34517127_34517128del	GRCh37
NC_000009.10:g.34507127_34507128del	NCBI36
NG_008127.1:g.63317_63318del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-156_1819-155del MANE Select	ENSP00000242317.4:n.1819-156_1819-155del
ENST00000242317.8:c.1819-156_1819-155del	ENSP00000242317.4:n.1819-156_1819-155del
ENST00000442556.1:c.329+2390_329+2391del
ENST00000470169.5:c.607-156_607-155del
ENST00000485580.1:n.395-156_395-155del
ENST00000614641.4:c.1831-156_1831-155del	ENSP00000480538.1:n.1831-156_1831-155del
NM_001281428.1:c.1831-156_1831-155del	NP_001268357.1:n.1831-156_1831-155del
NM_012144.3:c.1819-156_1819-155del	NP_036276.1:n.1819-156_1819-155del
XM_006716758.2:c.1288-156_1288-155del	XP_006716821.1:n.1288-156_1288-155del
XM_011517847.1:c.1831-66_1831-65del	XP_011516149.1:n.1831-66_1831-65del
XM_011517848.1:c.1573-156_1573-155del	XP_011516150.1:n.1573-156_1573-155del
XR_929233.1:n.1975-66_1975-65del
XM_006716758.3:c.1288-156_1288-155del	XP_006716821.1:n.1288-156_1288-155del
XM_011517847.3:c.1831-66_1831-65del	XP_011516149.1:n.1831-66_1831-65del
XM_011517848.2:c.1573-156_1573-155del	XP_011516150.1:n.1573-156_1573-155del
XM_017014625.2:c.1561-156_1561-155del	XP_016870114.1:n.1561-156_1561-155del
XR_002956774.1:n.1922-156_1922-155del
XR_929233.2:n.1922-66_1922-65del
NM_012144.4:c.1819-156_1819-155del MANE Select	NP_036276.1:n.1819-156_1819-155del
NM_001281428.2:c.1831-156_1831-155del	NP_001268357.1:n.1831-156_1831-155del