Canonical Allele Identifier: CA1845590952

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34517069A= , CM000671.2:g.34517069A=	GRCh38
NC_000009.11:g.34517067A= , CM000671.1:g.34517067A=	GRCh37
NC_000009.10:g.34507067A=	NCBI36
NG_008127.1:g.63257A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1819-216A= MANE Select	ENSP00000242317.4:n.1819-216A=
ENST00000242317.8:c.1819-216A=	ENSP00000242317.4:n.1819-216A=
ENST00000442556.1:c.329+2330A=
ENST00000470169.5:c.607-216A=
ENST00000485580.1:n.395-216A=
ENST00000614641.4:c.1831-216A=	ENSP00000480538.1:n.1831-216A=
NM_001281428.1:c.1831-216A=	NP_001268357.1:n.1831-216A=
NM_012144.3:c.1819-216A=	NP_036276.1:n.1819-216A=
XM_006716758.2:c.1288-216A=	XP_006716821.1:n.1288-216A=
XM_011517847.1:c.1831-126A=	XP_011516149.1:n.1831-126A=
XM_011517848.1:c.1573-216A=	XP_011516150.1:n.1573-216A=
XR_929233.1:n.1975-126A=
XM_006716758.3:c.1288-216A=	XP_006716821.1:n.1288-216A=
XM_011517847.3:c.1831-126A=	XP_011516149.1:n.1831-126A=
XM_011517848.2:c.1573-216A=	XP_011516150.1:n.1573-216A=
XM_017014625.2:c.1561-216A=	XP_016870114.1:n.1561-216A=
XR_002956774.1:n.1922-216A=
XR_929233.2:n.1922-126A=
NM_012144.4:c.1819-216A= MANE Select	NP_036276.1:n.1819-216A=
NM_001281428.2:c.1831-216A=	NP_001268357.1:n.1831-216A=