Canonical Allele Identifier: CA1845599112

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34506772C= , CM000671.2:g.34506772C=	GRCh38
NC_000009.11:g.34506770C= , CM000671.1:g.34506770C=	GRCh37
NC_000009.10:g.34496770C=	NCBI36
NG_008127.1:g.52960C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1209C= MANE Select	ENSP00000242317.4:p.His403=
ENST00000242317.8:c.1209C=	ENSP00000242317.4:p.His403=
ENST00000470169.5:c.146C=
ENST00000614641.4:c.1221C=	ENSP00000480538.1:p.His407=
NM_001281428.1:c.1221C=	NP_001268357.1:p.His407=
NM_012144.3:c.1209C=	NP_036276.1:p.His403=
XM_006716758.2:c.678C=	XP_006716821.1:p.His226=
XM_011517846.1:c.1221C=	XP_011516148.1:p.His407=
XM_011517847.1:c.1221C=	XP_011516149.1:p.His407=
XM_011517848.1:c.1221C=	XP_011516150.1:p.His407=
XM_011517849.1:c.1221C=	XP_011516151.1:p.His407=
XM_011517850.1:c.1221C=	XP_011516152.1:p.His407=
XR_929232.1:n.1475C=
XR_929233.1:n.1475C=
XR_929235.1:n.1475C=
XM_006716758.3:c.678C=	XP_006716821.1:p.His226=
XM_011517846.2:c.1221C=	XP_011516148.1:p.His407=
XM_011517847.3:c.1221C=	XP_011516149.1:p.His407=
XM_011517848.2:c.1221C=	XP_011516150.1:p.His407=
XM_011517849.2:c.1221C=	XP_011516151.1:p.His407=
XM_011517850.3:c.1221C=	XP_011516152.1:p.His407=
XM_017014625.2:c.1209C=	XP_016870114.1:p.His403=
XR_002956774.1:n.1422C=
XR_929232.2:n.1422C=
XR_929233.2:n.1422C=
NM_012144.4:c.1209C= MANE Select	NP_036276.1:p.His403=
NM_001281428.2:c.1221C=	NP_001268357.1:p.His407=