Canonical Allele Identifier: CA11377099

Gene: EEFSEC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.128319530C>A , CM000665.2:g.128319530C>A	GRCh38
NC_000003.11:g.128038373C>A , CM000665.1:g.128038373C>A	GRCh37
NC_000003.10:g.129521063C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254730.11:c.787-21703C>A MANE Select	ENSP00000254730.5:n.787-21703C>A
ENST00000254730.10:c.787-21703C>A	ENSP00000254730.5:n.787-21703C>A
ENST00000483457.1:c.622-21703C>A	ENSP00000417660.1:n.622-21703C>A
ENST00000484438.1:n.365-21703C>A
NM_021937.4:c.787-21703C>A	NP_068756.2:n.787-21703C>A
XM_005247696.1:c.622-21703C>A	XP_005247753.1:n.622-21703C>A
XM_011513063.1:c.787-21456C>A	XP_011511365.1:n.787-21456C>A
XM_011513064.1:c.787-21456C>A	XP_011511366.1:n.787-21456C>A
XM_011513065.1:c.787-21456C>A	XP_011511367.1:n.787-21456C>A
XM_005247696.3:c.622-21703C>A	XP_005247753.1:n.622-21703C>A
XM_011513066.2:c.-210-17374C>A	XP_011511368.1:n.-210-17374C>A
XM_024453692.1:c.787-21456C>A	XP_024309460.1:n.787-21456C>A
XM_024453693.1:c.787-21459C>A	XP_024309461.1:n.787-21459C>A
XM_024453694.1:c.787-21456C>A	XP_024309462.1:n.787-21456C>A
XM_024453695.1:c.787-21456C>A	XP_024309463.1:n.787-21456C>A
NM_021937.5:c.787-21703C>A MANE Select	NP_068756.2:n.787-21703C>A