Canonical Allele Identifier: CA371260826

Gene: CPA6 ARFGEF1-DT

Linked Data

• gnomAD v4: 8-67483795-T-A
• MyVariant Identifiers: chr8:g.68396030T>A (hg19) ; chr8:g.67483795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483795T>A , CM000670.2:g.67483795T>A	GRCh38
NC_000008.10:g.68396030T>A , CM000670.1:g.68396030T>A	GRCh37
NC_000008.9:g.68558584T>A	NCBI36
NG_027682.1:g.267591A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.811A>T (CPA6) MANE Select	ENSP00000297770.4:p.Asn271Tyr
ENST00000638254.1:c.*407A>T (CPA6)	ENSP00000491129.1:n.*407A>T
ENST00000297770.8:c.811A>T (CPA6)	ENSP00000297770.4:p.Asn271Tyr
ENST00000479862.6:c.*407A>T (CPA6)	ENSP00000419016.2:n.*407A>T
ENST00000518549.1:c.811A>T (CPA6)	ENSP00000431112.1:p.Asn271Tyr
NM_020361.4:c.811A>T (CPA6)	NP_065094.3:p.Asn271Tyr
XM_011517569.1:c.904A>T (CPA6)	XP_011515871.1:p.Asn302Tyr
XM_011517570.1:c.367A>T (CPA6)	XP_011515872.1:p.Asn123Tyr
NR_136224.1:n.694-7170T>A (ARFGEF1-DT)
XM_011517570.2:c.367A>T (CPA6)	XP_011515872.1:p.Asn123Tyr
XM_017013646.1:c.367A>T (CPA6)	XP_016869135.1:p.Asn123Tyr
XR_001745565.1:n.1619A>T (CPA6)
NM_020361.5:c.811A>T (CPA6) MANE Select	NP_065094.3:p.Asn271Tyr