Canonical Allele Identifier: CA371260902

Gene: CPA6 ARFGEF1-DT

Linked Data

• gnomAD v4: 8-67483833-G-C
• MyVariant Identifiers: chr8:g.68396068G>C (hg19) ; chr8:g.67483833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483833G>C , CM000670.2:g.67483833G>C	GRCh38
NC_000008.10:g.68396068G>C , CM000670.1:g.68396068G>C	GRCh37
NC_000008.9:g.68558622G>C	NCBI36
NG_027682.1:g.267553C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.773C>G (CPA6) MANE Select	ENSP00000297770.4:p.Ser258Ter
ENST00000638254.1:c.*369C>G (CPA6)	ENSP00000491129.1:n.*369C>G
ENST00000297770.8:c.773C>G (CPA6)	ENSP00000297770.4:p.Ser258Ter
ENST00000479862.6:c.*369C>G (CPA6)	ENSP00000419016.2:n.*369C>G
ENST00000518549.1:c.773C>G (CPA6)	ENSP00000431112.1:p.Ser258Ter
NM_020361.4:c.773C>G (CPA6)	NP_065094.3:p.Ser258Ter
XM_011517569.1:c.866C>G (CPA6)	XP_011515871.1:p.Ser289Ter
XM_011517570.1:c.329C>G (CPA6)	XP_011515872.1:p.Ser110Ter
NR_136224.1:n.694-7132G>C (ARFGEF1-DT)
XM_011517570.2:c.329C>G (CPA6)	XP_011515872.1:p.Ser110Ter
XM_017013646.1:c.329C>G (CPA6)	XP_016869135.1:p.Ser110Ter
XR_001745565.1:n.1581C>G (CPA6)
NM_020361.5:c.773C>G (CPA6) MANE Select	NP_065094.3:p.Ser258Ter