Canonical Allele Identifier: CA371260876

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68396056C>A (hg19) ; chr8:g.67483821C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483821C>A , CM000670.2:g.67483821C>A	GRCh38
NC_000008.10:g.68396056C>A , CM000670.1:g.68396056C>A	GRCh37
NC_000008.9:g.68558610C>A	NCBI36
NG_027682.1:g.267565G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.785G>T (CPA6) MANE Select	ENSP00000297770.4:p.Arg262Met
ENST00000638254.1:c.*381G>T (CPA6)	ENSP00000491129.1:n.*381G>T
ENST00000297770.8:c.785G>T (CPA6)	ENSP00000297770.4:p.Arg262Met
ENST00000479862.6:c.*381G>T (CPA6)	ENSP00000419016.2:n.*381G>T
ENST00000518549.1:c.785G>T (CPA6)	ENSP00000431112.1:p.Arg262Met
NM_020361.4:c.785G>T (CPA6)	NP_065094.3:p.Arg262Met
XM_011517569.1:c.878G>T (CPA6)	XP_011515871.1:p.Arg293Met
XM_011517570.1:c.341G>T (CPA6)	XP_011515872.1:p.Arg114Met
NR_136224.1:n.694-7144C>A (ARFGEF1-DT)
XM_011517570.2:c.341G>T (CPA6)	XP_011515872.1:p.Arg114Met
XM_017013646.1:c.341G>T (CPA6)	XP_016869135.1:p.Arg114Met
XR_001745565.1:n.1593G>T (CPA6)
NM_020361.5:c.785G>T (CPA6) MANE Select	NP_065094.3:p.Arg262Met