Canonical Allele Identifier: CA863462599

Gene: DNAI1

Linked Data

• dbSNP Id: rs1177362036
• MyVariant Identifiers: chr9:g.34517090del (hg19) ; chr9:g.34517092del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517092del , CM000671.2:g.34517092del	GRCh38
NC_000009.11:g.34517090del , CM000671.1:g.34517090del	GRCh37
NC_000009.10:g.34507090del	NCBI36
NG_008127.1:g.63280del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-193del MANE Select	ENSP00000242317.4:n.1819-193del
ENST00000242317.8:c.1819-193del	ENSP00000242317.4:n.1819-193del
ENST00000442556.1:c.329+2353del
ENST00000470169.5:c.607-193del
ENST00000485580.1:n.395-193del
ENST00000614641.4:c.1831-193del	ENSP00000480538.1:n.1831-193del
NM_001281428.1:c.1831-193del	NP_001268357.1:n.1831-193del
NM_012144.3:c.1819-193del	NP_036276.1:n.1819-193del
XM_006716758.2:c.1288-193del	XP_006716821.1:n.1288-193del
XM_011517847.1:c.1831-103del	XP_011516149.1:n.1831-103del
XM_011517848.1:c.1573-193del	XP_011516150.1:n.1573-193del
XR_929233.1:n.1975-103del
XM_006716758.3:c.1288-193del	XP_006716821.1:n.1288-193del
XM_011517847.3:c.1831-103del	XP_011516149.1:n.1831-103del
XM_011517848.2:c.1573-193del	XP_011516150.1:n.1573-193del
XM_017014625.2:c.1561-193del	XP_016870114.1:n.1561-193del
XR_002956774.1:n.1922-193del
XR_929233.2:n.1922-103del
NM_012144.4:c.1819-193del MANE Select	NP_036276.1:n.1819-193del
NM_001281428.2:c.1831-193del	NP_001268357.1:n.1831-193del