Canonical Allele Identifier: CA1845599261

Gene: DNAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34506809C= , CM000671.2:g.34506809C=	GRCh38
NC_000009.11:g.34506807C= , CM000671.1:g.34506807C=	GRCh37
NC_000009.10:g.34496807C=	NCBI36
NG_008127.1:g.52997C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000242317.9:c.1246C= MANE Select	ENSP00000242317.4:p.Pro416=
ENST00000242317.8:c.1246C=	ENSP00000242317.4:p.Pro416=
ENST00000470169.5:c.183C=
ENST00000614641.4:c.1258C=	ENSP00000480538.1:p.Pro420=
NM_001281428.1:c.1258C=	NP_001268357.1:p.Pro420=
NM_012144.3:c.1246C=	NP_036276.1:p.Pro416=
XM_006716758.2:c.715C=	XP_006716821.1:p.Pro239=
XM_011517846.1:c.1258C=	XP_011516148.1:p.Pro420=
XM_011517847.1:c.1258C=	XP_011516149.1:p.Pro420=
XM_011517848.1:c.1258C=	XP_011516150.1:p.Pro420=
XM_011517849.1:c.1258C=	XP_011516151.1:p.Pro420=
XM_011517850.1:c.1258C=	XP_011516152.1:p.Pro420=
XR_929232.1:n.1512C=
XR_929233.1:n.1512C=
XR_929235.1:n.1512C=
XM_006716758.3:c.715C=	XP_006716821.1:p.Pro239=
XM_011517846.2:c.1258C=	XP_011516148.1:p.Pro420=
XM_011517847.3:c.1258C=	XP_011516149.1:p.Pro420=
XM_011517848.2:c.1258C=	XP_011516150.1:p.Pro420=
XM_011517849.2:c.1258C=	XP_011516151.1:p.Pro420=
XM_011517850.3:c.1258C=	XP_011516152.1:p.Pro420=
XM_017014625.2:c.1246C=	XP_016870114.1:p.Pro416=
XR_002956774.1:n.1459C=
XR_929232.2:n.1459C=
XR_929233.2:n.1459C=
NM_012144.4:c.1246C= MANE Select	NP_036276.1:p.Pro416=
NM_001281428.2:c.1258C=	NP_001268357.1:p.Pro420=