Canonical Allele Identifier: CA1845591019

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517096T= , CM000671.2:g.34517096T=	GRCh38
NC_000009.11:g.34517094T= , CM000671.1:g.34517094T=	GRCh37
NC_000009.10:g.34507094T=	NCBI36
NG_008127.1:g.63284T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-189T= MANE Select	ENSP00000242317.4:n.1819-189T=
ENST00000242317.8:c.1819-189T=	ENSP00000242317.4:n.1819-189T=
ENST00000442556.1:c.329+2357T=
ENST00000470169.5:c.607-189T=
ENST00000485580.1:n.395-189T=
ENST00000614641.4:c.1831-189T=	ENSP00000480538.1:n.1831-189T=
NM_001281428.1:c.1831-189T=	NP_001268357.1:n.1831-189T=
NM_012144.3:c.1819-189T=	NP_036276.1:n.1819-189T=
XM_006716758.2:c.1288-189T=	XP_006716821.1:n.1288-189T=
XM_011517847.1:c.1831-99T=	XP_011516149.1:n.1831-99T=
XM_011517848.1:c.1573-189T=	XP_011516150.1:n.1573-189T=
XR_929233.1:n.1975-99T=
XM_006716758.3:c.1288-189T=	XP_006716821.1:n.1288-189T=
XM_011517847.3:c.1831-99T=	XP_011516149.1:n.1831-99T=
XM_011517848.2:c.1573-189T=	XP_011516150.1:n.1573-189T=
XM_017014625.2:c.1561-189T=	XP_016870114.1:n.1561-189T=
XR_002956774.1:n.1922-189T=
XR_929233.2:n.1922-99T=
NM_012144.4:c.1819-189T= MANE Select	NP_036276.1:n.1819-189T=
NM_001281428.2:c.1831-189T=	NP_001268357.1:n.1831-189T=