Canonical Allele Identifier: CA378970744

Gene: EPS8L2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.722137T>A , CM000673.2:g.722137T>A	GRCh38
NC_000011.9:g.722137T>A , CM000673.1:g.722137T>A	GRCh37
NC_000011.8:g.712137T>A	NCBI36
NG_051601.1:g.21921T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000318562.13:c.1031T>A MANE Select	ENSP00000320828.8:p.Val344Glu
ENST00000650127.1:c.1031T>A	ENSP00000497389.1:p.Val344Glu
ENST00000318562.12:c.1031T>A	ENSP00000320828.8:p.Val344Glu
ENST00000524474.5:n.695T>A
ENST00000526198.5:c.1079T>A	ENSP00000436230.1:p.Val360Glu
ENST00000526651.5:n.472+146T>A
ENST00000526909.5:c.*1736T>A	ENSP00000433173.1:n.*1736T>A
ENST00000528770.5:c.374T>A
ENST00000529346.5:n.1553T>A
ENST00000530452.6:c.318-264T>A
ENST00000530636.5:c.1031T>A	ENSP00000436035.1:p.Val344Glu
ENST00000531393.5:n.212T>A
ENST00000533256.5:c.1031T>A	ENSP00000435585.1:p.Val344Glu
ENST00000533816.1:n.334T>A
ENST00000610855.4:c.-369T>A	ENSP00000480704.1:n.-369T>A
ENST00000614442.4:c.1079T>A	ENSP00000480201.1:p.Val360Glu
NM_022772.3:c.1031T>A	NP_073609.2:p.Val344Glu
XM_017018131.1:c.1031T>A	XP_016873620.1:p.Val344Glu
XM_017018132.1:c.1031T>A	XP_016873621.1:p.Val344Glu
NM_022772.4:c.1031T>A MANE Select	NP_073609.2:p.Val344Glu