Canonical Allele Identifier: CA1017981018

Gene: EYA2

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46999130C>A , CM000682.2:g.46999130C>A	GRCh38
NC_000020.10:g.45627769C>A , CM000682.1:g.45627769C>A	GRCh37
NC_000020.9:g.45061176C>A	NCBI36
NG_011673.1:g.109261C>A
NG_011673.2:g.109261C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327619.10:c.110-2298C>A MANE Select	ENSP00000333640.5:n.110-2298C>A
ENST00000317304.10:c.110-2298C>A	ENSP00000321590.6:n.110-2298C>A
ENST00000327619.9:c.110-2298C>A	ENSP00000333640.5:n.110-2298C>A
ENST00000357410.7:c.110-2298C>A	ENSP00000349986.3:n.110-2298C>A
ENST00000497062.6:c.110-2298C>A	ENSP00000417105.3:n.110-2298C>A
ENST00000611592.4:c.110-2298C>A	ENSP00000483392.1:n.110-2298C>A
NM_005244.4:c.110-2298C>A	NP_005235.3:n.110-2298C>A
NM_172110.3:c.110-2298C>A	NP_742108.2:n.110-2298C>A
XM_005260327.1:c.110-2298C>A	XP_005260384.1:n.110-2298C>A
XM_011528687.1:c.110-2298C>A	XP_011526989.1:n.110-2298C>A
XM_005260327.2:c.110-2298C>A	XP_005260384.1:n.110-2298C>A
XM_017027721.2:c.110-2298C>A	XP_016883210.1:n.110-2298C>A
NM_005244.5:c.110-2298C>A MANE Select	NP_005235.3:n.110-2298C>A
NM_172110.4:c.110-2298C>A	NP_742108.2:n.110-2298C>A