Canonical Allele Identifier: CA2838298942

Gene: SEC22A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.123237816A>C , CM000665.2:g.123237816A>C	GRCh38
NC_000003.11:g.122956663A>C , CM000665.1:g.122956663A>C	GRCh37
NC_000003.10:g.124439353A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000492595.6:c.542-8083A>C MANE Select	ENSP00000417972.1:n.542-8083A>C
ENST00000309934.4:c.542-8083A>C	ENSP00000310521.4:n.542-8083A>C
ENST00000466950.5:c.*241-8083A>C	ENSP00000417200.1:n.*241-8083A>C
ENST00000473494.6:c.542-8083A>C	ENSP00000420343.2:n.542-8083A>C
ENST00000477063.5:n.621-5996A>C
ENST00000481965.6:c.183-21708A>C	ENSP00000420128.2:n.183-21708A>C
ENST00000487572.5:c.542-8083A>C	ENSP00000420015.1:n.542-8083A>C
ENST00000492595.5:c.542-8083A>C	ENSP00000417972.1:n.542-8083A>C
NM_012430.4:c.542-8083A>C	NP_036562.2:n.542-8083A>C
XM_011512673.1:c.542-8083A>C	XP_011510975.1:n.542-8083A>C
XM_011512674.1:c.542-8083A>C	XP_011510976.1:n.542-8083A>C
XM_011512675.1:c.542-8083A>C	XP_011510977.1:n.542-8083A>C
XM_011512676.1:c.542-8083A>C	XP_011510978.1:n.542-8083A>C
XM_011512673.3:c.542-8083A>C	XP_011510975.1:n.542-8083A>C
XM_011512675.3:c.542-8083A>C	XP_011510977.1:n.542-8083A>C
XM_011512676.3:c.542-8083A>C	XP_011510978.1:n.542-8083A>C
NM_012430.5:c.542-8083A>C MANE Select	NP_036562.2:n.542-8083A>C