Canonical Allele Identifier: CA1845608516

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34513035C= , CM000671.2:g.34513035C=	GRCh38
NC_000009.11:g.34513033C= , CM000671.1:g.34513033C=	GRCh37
NC_000009.10:g.34503033C=	NCBI36
NG_008127.1:g.59223C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1490-77C= MANE Select	ENSP00000242317.4:n.1490-77C=
ENST00000242317.8:c.1490-77C=	ENSP00000242317.4:n.1490-77C=
ENST00000470169.5:c.427-77C=
ENST00000614641.4:c.1502-77C=	ENSP00000480538.1:n.1502-77C=
NM_001281428.1:c.1502-77C=	NP_001268357.1:n.1502-77C=
NM_012144.3:c.1490-77C=	NP_036276.1:n.1490-77C=
XM_006716758.2:c.959-77C=	XP_006716821.1:n.959-77C=
XM_011517846.1:c.1502-77C=	XP_011516148.1:n.1502-77C=
XM_011517847.1:c.1502-77C=	XP_011516149.1:n.1502-77C=
XM_011517848.1:c.1324-1359C=	XP_011516150.1:n.1324-1359C=
XM_011517849.1:c.1502-77C=	XP_011516151.1:n.1502-77C=
XR_929232.1:n.1756-77C=
XR_929233.1:n.1756-77C=
XR_929235.1:n.1578-1469C=
XM_006716758.3:c.959-77C=	XP_006716821.1:n.959-77C=
XM_011517846.2:c.1502-77C=	XP_011516148.1:n.1502-77C=
XM_011517847.3:c.1502-77C=	XP_011516149.1:n.1502-77C=
XM_011517848.2:c.1324-1359C=	XP_011516150.1:n.1324-1359C=
XM_011517849.2:c.1502-77C=	XP_011516151.1:n.1502-77C=
XM_017014625.2:c.1312-1359C=	XP_016870114.1:n.1312-1359C=
XR_002956774.1:n.1703-77C=
XR_929232.2:n.1703-77C=
XR_929233.2:n.1703-77C=
NM_012144.4:c.1490-77C= MANE Select	NP_036276.1:n.1490-77C=
NM_001281428.2:c.1502-77C=	NP_001268357.1:n.1502-77C=