Canonical Allele Identifier: CA2830535927

Gene: SEC62

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169977240dup , CM000665.2:g.169977240dup	GRCh38
NC_000003.11:g.169695028dup , CM000665.1:g.169695028dup	GRCh37
NC_000003.10:g.171177722dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337002.9:c.251+189dup MANE Select	ENSP00000337688.4:n.251+189dup
ENST00000337002.8:c.251+189dup	ENSP00000337688.4:n.251+189dup
ENST00000460513.5:c.251+189dup	ENSP00000419319.1:n.251+189dup
ENST00000469515.6:c.251+189dup	ENSP00000418342.2:n.251+189dup
ENST00000480708.5:c.251+189dup	ENSP00000420331.1:n.251+189dup
ENST00000481435.5:n.248+189dup
ENST00000487736.5:c.*204+189dup	ENSP00000420304.1:n.*204+189dup
ENST00000497277.1:n.372+189dup
NM_003262.3:c.251+189dup	NP_003253.1:n.251+189dup
XM_011513114.1:c.137+189dup	XP_011511416.1:n.137+189dup
XM_011513114.3:c.137+189dup	XP_011511416.1:n.137+189dup
NM_003262.4:c.251+189dup MANE Select	NP_003253.1:n.251+189dup