Canonical Allele Identifier: CA400909193

Gene: DNAI2

Linked Data

• MyVariant Identifiers: chr17:g.72297231T>G (hg19) ; chr17:g.74301092T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74301092T>G , CM000679.2:g.74301092T>G	GRCh38
NC_000017.10:g.72297231T>G , CM000679.1:g.72297231T>G	GRCh37
NC_000017.9:g.69808826T>G	NCBI36
NG_016865.1:g.31846T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311014.11:c.911T>G MANE Select	ENSP00000308312.6:p.Val304Gly
ENST00000311014.10:c.911T>G	ENSP00000308312.6:p.Val304Gly
ENST00000446837.2:c.911T>G	ENSP00000400252.2:p.Val304Gly
ENST00000579055.5:c.*282T>G	ENSP00000462767.1:n.*282T>G
ENST00000579490.5:c.1082T>G	ENSP00000464197.1:p.Val361Gly
ENST00000582036.5:c.911T>G	ENSP00000461950.1:p.Val304Gly
NM_001172810.1:c.911T>G	NP_001166281.1:p.Val304Gly
NM_023036.4:c.911T>G	NP_075462.3:p.Val304Gly
XM_011525125.1:c.911T>G	XP_011523427.1:p.Val304Gly
XR_429915.2:n.1033T>G
XR_429916.2:n.1033T>G
XR_934518.1:n.1035T>G
XR_934519.1:n.1032T>G
XR_934520.1:n.1108T>G
XR_934521.1:n.1020T>G
XR_934522.1:n.1008T>G
XR_934523.1:n.1017T>G
XR_934524.1:n.1035T>G
XR_934525.1:n.1035T>G
XR_934526.1:n.921T>G
XR_934527.1:n.1033T>G
XR_934528.1:n.1033T>G
XR_934529.1:n.914T>G
XR_934530.1:n.987T>G
XR_934531.1:n.913T>G
NM_001172810.2:c.911T>G	NP_001166281.1:p.Val304Gly
NM_001353167.1:c.911T>G	NP_001340096.1:p.Val304Gly
NM_023036.5:c.911T>G	NP_075462.3:p.Val304Gly
NR_148379.1:n.936T>G
XM_011525125.2:c.911T>G	XP_011523427.1:p.Val304Gly
XM_024450874.1:c.911T>G	XP_024306642.1:p.Val304Gly
XM_024450875.1:c.911T>G	XP_024306643.1:p.Val304Gly
XM_024450876.1:c.911T>G	XP_024306644.1:p.Val304Gly
XM_024450877.1:c.911T>G	XP_024306645.1:p.Val304Gly
XM_024450878.1:c.911T>G	XP_024306646.1:p.Val304Gly
XM_024450879.1:c.911T>G	XP_024306647.1:p.Val304Gly
XM_024450880.1:c.911T>G	XP_024306648.1:p.Val304Gly
XM_024450881.1:c.797T>G	XP_024306649.1:p.Val266Gly
XM_024450882.1:c.911T>G	XP_024306650.1:p.Val304Gly
XM_024450883.1:c.911T>G	XP_024306651.1:p.Val304Gly
XM_024450884.1:c.911T>G	XP_024306652.1:p.Val304Gly
XM_024450885.1:c.482T>G	XP_024306653.1:p.Val161Gly
XM_024450886.1:c.482T>G	XP_024306654.1:p.Val161Gly
NM_023036.6:c.911T>G MANE Select	NP_075462.3:p.Val304Gly
NM_001172810.3:c.911T>G	NP_001166281.1:p.Val304Gly
NM_001353167.2:c.911T>G	NP_001340096.1:p.Val304Gly
NR_148379.2:n.912T>G