Canonical Allele Identifier: CA2830535928

Gene: SEC62

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169977243A>G , CM000665.2:g.169977243A>G	GRCh38
NC_000003.11:g.169695031A>G , CM000665.1:g.169695031A>G	GRCh37
NC_000003.10:g.171177725A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337002.9:c.251+192A>G MANE Select	ENSP00000337688.4:n.251+192A>G
ENST00000337002.8:c.251+192A>G	ENSP00000337688.4:n.251+192A>G
ENST00000460513.5:c.251+192A>G	ENSP00000419319.1:n.251+192A>G
ENST00000469515.6:c.251+192A>G	ENSP00000418342.2:n.251+192A>G
ENST00000480708.5:c.251+192A>G	ENSP00000420331.1:n.251+192A>G
ENST00000481435.5:n.248+192A>G
ENST00000487736.5:c.*204+192A>G	ENSP00000420304.1:n.*204+192A>G
ENST00000497277.1:n.372+192A>G
NM_003262.3:c.251+192A>G	NP_003253.1:n.251+192A>G
XM_011513114.1:c.137+192A>G	XP_011511416.1:n.137+192A>G
XM_011513114.3:c.137+192A>G	XP_011511416.1:n.137+192A>G
NM_003262.4:c.251+192A>G MANE Select	NP_003253.1:n.251+192A>G