Canonical Allele Identifier: CA371260846

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68396039C>T (hg19) ; chr8:g.67483804C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483804C>T , CM000670.2:g.67483804C>T	GRCh38
NC_000008.10:g.68396039C>T , CM000670.1:g.68396039C>T	GRCh37
NC_000008.9:g.68558593C>T	NCBI36
NG_027682.1:g.267582G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.802G>A (CPA6) MANE Select	ENSP00000297770.4:p.Val268Met
ENST00000638254.1:c.*398G>A (CPA6)	ENSP00000491129.1:n.*398G>A
ENST00000297770.8:c.802G>A (CPA6)	ENSP00000297770.4:p.Val268Met
ENST00000479862.6:c.*398G>A (CPA6)	ENSP00000419016.2:n.*398G>A
ENST00000518549.1:c.802G>A (CPA6)	ENSP00000431112.1:p.Val268Met
NM_020361.4:c.802G>A (CPA6)	NP_065094.3:p.Val268Met
XM_011517569.1:c.895G>A (CPA6)	XP_011515871.1:p.Val299Met
XM_011517570.1:c.358G>A (CPA6)	XP_011515872.1:p.Val120Met
NR_136224.1:n.694-7161C>T (ARFGEF1-DT)
XM_011517570.2:c.358G>A (CPA6)	XP_011515872.1:p.Val120Met
XM_017013646.1:c.358G>A (CPA6)	XP_016869135.1:p.Val120Met
XR_001745565.1:n.1610G>A (CPA6)
NM_020361.5:c.802G>A (CPA6) MANE Select	NP_065094.3:p.Val268Met