Canonical Allele Identifier: CA1845610401

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34514441C= , CM000671.2:g.34514441C=	GRCh38
NC_000009.11:g.34514439C= , CM000671.1:g.34514439C=	GRCh37
NC_000009.10:g.34504439C=	NCBI36
NG_008127.1:g.60629C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1617C= MANE Select	ENSP00000242317.4:p.His539=
ENST00000242317.8:c.1617C=	ENSP00000242317.4:p.His539=
ENST00000442556.1:c.128C=
ENST00000470169.5:c.507-199C=
ENST00000485580.1:n.96C=
ENST00000614641.4:c.1629C=	ENSP00000480538.1:p.His543=
NM_001281428.1:c.1629C=	NP_001268357.1:p.His543=
NM_012144.3:c.1617C=	NP_036276.1:p.His539=
XM_006716758.2:c.1086C=	XP_006716821.1:p.His362=
XM_011517846.1:c.1629C=	XP_011516148.1:p.His543=
XM_011517847.1:c.1629C=	XP_011516149.1:p.His543=
XM_011517848.1:c.1371C=	XP_011516150.1:p.His457=
XM_011517849.1:c.1582-63C=	XP_011516151.1:n.1582-63C=
XR_929232.1:n.1836-63C=
XR_929233.1:n.1836-63C=
XR_929235.1:n.1578-63C=
XM_006716758.3:c.1086C=	XP_006716821.1:p.His362=
XM_011517846.2:c.1629C=	XP_011516148.1:p.His543=
XM_011517847.3:c.1629C=	XP_011516149.1:p.His543=
XM_011517848.2:c.1371C=	XP_011516150.1:p.His457=
XM_011517849.2:c.1582-63C=	XP_011516151.1:n.1582-63C=
XM_017014625.2:c.1359C=	XP_016870114.1:p.His453=
XR_002956774.1:n.1783-63C=
XR_929232.2:n.1783-63C=
XR_929233.2:n.1783-63C=
NM_012144.4:c.1617C= MANE Select	NP_036276.1:p.His539=
NM_001281428.2:c.1629C=	NP_001268357.1:p.His543=