Canonical Allele Identifier: CA2274958332

Gene: DNAI2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74301057G= , CM000679.2:g.74301057G=	GRCh38
NC_000017.10:g.72297196G= , CM000679.1:g.72297196G=	GRCh37
NC_000017.9:g.69808791G=	NCBI36
NG_016865.1:g.31811G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311014.11:c.876G= MANE Select	ENSP00000308312.6:p.Trp292=
ENST00000311014.10:c.876G=	ENSP00000308312.6:p.Trp292=
ENST00000446837.2:c.876G=	ENSP00000400252.2:p.Trp292=
ENST00000579055.5:c.*247G=	ENSP00000462767.1:n.*247G=
ENST00000579490.5:c.1047G=	ENSP00000464197.1:p.Trp349=
ENST00000582036.5:c.876G=	ENSP00000461950.1:p.Trp292=
NM_001172810.1:c.876G=	NP_001166281.1:p.Trp292=
NM_023036.4:c.876G=	NP_075462.3:p.Trp292=
XM_011525125.1:c.876G=	XP_011523427.1:p.Trp292=
XR_429915.2:n.998G=
XR_429916.2:n.998G=
XR_934518.1:n.1000G=
XR_934519.1:n.997G=
XR_934520.1:n.1073G=
XR_934521.1:n.985G=
XR_934522.1:n.973G=
XR_934523.1:n.982G=
XR_934524.1:n.1000G=
XR_934525.1:n.1000G=
XR_934526.1:n.886G=
XR_934527.1:n.998G=
XR_934528.1:n.998G=
XR_934529.1:n.879G=
XR_934530.1:n.952G=
XR_934531.1:n.878G=
NM_001172810.2:c.876G=	NP_001166281.1:p.Trp292=
NM_001353167.1:c.876G=	NP_001340096.1:p.Trp292=
NM_023036.5:c.876G=	NP_075462.3:p.Trp292=
NR_148379.1:n.901G=
XM_011525125.2:c.876G=	XP_011523427.1:p.Trp292=
XM_024450874.1:c.876G=	XP_024306642.1:p.Trp292=
XM_024450875.1:c.876G=	XP_024306643.1:p.Trp292=
XM_024450876.1:c.876G=	XP_024306644.1:p.Trp292=
XM_024450877.1:c.876G=	XP_024306645.1:p.Trp292=
XM_024450878.1:c.876G=	XP_024306646.1:p.Trp292=
XM_024450879.1:c.876G=	XP_024306647.1:p.Trp292=
XM_024450880.1:c.876G=	XP_024306648.1:p.Trp292=
XM_024450881.1:c.762G=	XP_024306649.1:p.Trp254=
XM_024450882.1:c.876G=	XP_024306650.1:p.Trp292=
XM_024450883.1:c.876G=	XP_024306651.1:p.Trp292=
XM_024450884.1:c.876G=	XP_024306652.1:p.Trp292=
XM_024450885.1:c.447G=	XP_024306653.1:p.Trp149=
XM_024450886.1:c.447G=	XP_024306654.1:p.Trp149=
NM_023036.6:c.876G= MANE Select	NP_075462.3:p.Trp292=
NM_001172810.3:c.876G=	NP_001166281.1:p.Trp292=
NM_001353167.2:c.876G=	NP_001340096.1:p.Trp292=
NR_148379.2:n.877G=