Canonical Allele Identifier: CA148936717

Gene: ADGB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.146734022G>A , CM000668.2:g.146734022G>A	GRCh38
NC_000006.11:g.147055158G>A , CM000668.1:g.147055158G>A	GRCh37
NC_000006.10:g.147096851G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_024694.4:c.2786G>A MANE Select	NP_078970.3:p.Arg929Lys
ENST00000397944.8:c.2786G>A MANE Select	ENSP00000381036.3:p.Arg929Lys
NM_024694.3:c.2786G>A	NP_078970.3:p.Arg929Lys
ENST00000397944.7:c.2786G>A	ENSP00000381036.3:p.Arg929Lys
ENST00000480328.6:c.1045G>A
ENST00000493950.6:c.*3617G>A	ENSP00000430244.1:n.*3617G>A
ENST00000681847.1:c.2786G>A	ENSP00000505524.1:p.Arg929Lys
XM_006715566.2:c.2786G>A	XP_006715629.1:p.Arg929Lys
XM_006715566.4:c.2786G>A	XP_006715629.1:p.Arg929Lys
XM_011536125.1:c.2768G>A	XP_011534427.1:p.Arg923Lys
XM_011536125.3:c.2768G>A	XP_011534427.1:p.Arg923Lys
XM_011536126.1:c.2786G>A	XP_011534428.1:p.Arg929Lys
XM_011536127.1:c.2786G>A	XP_011534429.1:p.Arg929Lys
XM_011536127.3:c.2786G>A	XP_011534429.1:p.Arg929Lys
XM_011536128.1:c.2786G>A	XP_011534430.1:p.Arg929Lys
XM_011536128.3:c.2786G>A	XP_011534430.1:p.Arg929Lys
XM_011536129.1:c.2381G>A	XP_011534431.1:p.Arg794Lys
XM_011536130.1:c.2381G>A	XP_011534432.1:p.Arg794Lys
XM_011536130.3:c.2381G>A	XP_011534432.1:p.Arg794Lys
XM_011536131.1:c.1937G>A	XP_011534433.1:p.Arg646Lys
XM_011536131.3:c.1937G>A	XP_011534433.1:p.Arg646Lys
XM_011536132.1:c.1544G>A	XP_011534434.1:p.Arg515Lys
XM_011536132.3:c.1544G>A	XP_011534434.1:p.Arg515Lys
XM_011536133.1:c.2786G>A	XP_011534435.1:p.Arg929Lys
XM_011536134.1:c.542G>A	XP_011534436.1:p.Arg181Lys
XM_011536134.3:c.542G>A	XP_011534436.1:p.Arg181Lys
XM_011536135.1:c.398G>A	XP_011534437.1:p.Arg133Lys
XM_011536135.3:c.398G>A	XP_011534437.1:p.Arg133Lys
XM_017011315.2:c.2786G>A	XP_016866804.1:p.Arg929Lys
XM_024446552.1:c.2381G>A	XP_024302320.1:p.Arg794Lys
XR_943093.1:n.451+1275C>T