Canonical Allele Identifier: CA2274958334

Gene: DNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74301064C= , CM000679.2:g.74301064C=	GRCh38
NC_000017.10:g.72297203C= , CM000679.1:g.72297203C=	GRCh37
NC_000017.9:g.69808798C=	NCBI36
NG_016865.1:g.31818C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311014.11:c.883C= MANE Select	ENSP00000308312.6:p.Arg295=
ENST00000311014.10:c.883C=	ENSP00000308312.6:p.Arg295=
ENST00000446837.2:c.883C=	ENSP00000400252.2:p.Arg295=
ENST00000579055.5:c.*254C=	ENSP00000462767.1:n.*254C=
ENST00000579490.5:c.1054C=	ENSP00000464197.1:p.Arg352=
ENST00000582036.5:c.883C=	ENSP00000461950.1:p.Arg295=
NM_001172810.1:c.883C=	NP_001166281.1:p.Arg295=
NM_023036.4:c.883C=	NP_075462.3:p.Arg295=
XM_011525125.1:c.883C=	XP_011523427.1:p.Arg295=
XR_429915.2:n.1005C=
XR_429916.2:n.1005C=
XR_934518.1:n.1007C=
XR_934519.1:n.1004C=
XR_934520.1:n.1080C=
XR_934521.1:n.992C=
XR_934522.1:n.980C=
XR_934523.1:n.989C=
XR_934524.1:n.1007C=
XR_934525.1:n.1007C=
XR_934526.1:n.893C=
XR_934527.1:n.1005C=
XR_934528.1:n.1005C=
XR_934529.1:n.886C=
XR_934530.1:n.959C=
XR_934531.1:n.885C=
NM_001172810.2:c.883C=	NP_001166281.1:p.Arg295=
NM_001353167.1:c.883C=	NP_001340096.1:p.Arg295=
NM_023036.5:c.883C=	NP_075462.3:p.Arg295=
NR_148379.1:n.908C=
XM_011525125.2:c.883C=	XP_011523427.1:p.Arg295=
XM_024450874.1:c.883C=	XP_024306642.1:p.Arg295=
XM_024450875.1:c.883C=	XP_024306643.1:p.Arg295=
XM_024450876.1:c.883C=	XP_024306644.1:p.Arg295=
XM_024450877.1:c.883C=	XP_024306645.1:p.Arg295=
XM_024450878.1:c.883C=	XP_024306646.1:p.Arg295=
XM_024450879.1:c.883C=	XP_024306647.1:p.Arg295=
XM_024450880.1:c.883C=	XP_024306648.1:p.Arg295=
XM_024450881.1:c.769C=	XP_024306649.1:p.Arg257=
XM_024450882.1:c.883C=	XP_024306650.1:p.Arg295=
XM_024450883.1:c.883C=	XP_024306651.1:p.Arg295=
XM_024450884.1:c.883C=	XP_024306652.1:p.Arg295=
XM_024450885.1:c.454C=	XP_024306653.1:p.Arg152=
XM_024450886.1:c.454C=	XP_024306654.1:p.Arg152=
NM_023036.6:c.883C= MANE Select	NP_075462.3:p.Arg295=
NM_001172810.3:c.883C=	NP_001166281.1:p.Arg295=
NM_001353167.2:c.883C=	NP_001340096.1:p.Arg295=
NR_148379.2:n.884C=