Canonical Allele Identifier: CA461344259

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68396037C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483802C>T , CM000670.2:g.67483802C>T	GRCh38
NC_000008.10:g.68396037C>T , CM000670.1:g.68396037C>T	GRCh37
NC_000008.9:g.68558591C>T	NCBI36
NG_027682.1:g.267584G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.804G>A (CPA6) MANE Select	ENSP00000297770.4:p.Val268=
ENST00000638254.1:c.*400G>A (CPA6)	ENSP00000491129.1:n.*400G>A
ENST00000297770.8:c.804G>A (CPA6)	ENSP00000297770.4:p.Val268=
ENST00000479862.6:c.*400G>A (CPA6)	ENSP00000419016.2:n.*400G>A
ENST00000518549.1:c.804G>A (CPA6)	ENSP00000431112.1:p.Val268=
NM_020361.4:c.804G>A (CPA6)	NP_065094.3:p.Val268=
XM_011517569.1:c.897G>A (CPA6)	XP_011515871.1:p.Val299=
XM_011517570.1:c.360G>A (CPA6)	XP_011515872.1:p.Val120=
NR_136224.1:n.694-7163C>T (ARFGEF1-DT)
XM_011517570.2:c.360G>A (CPA6)	XP_011515872.1:p.Val120=
XM_017013646.1:c.360G>A (CPA6)	XP_016869135.1:p.Val120=
XR_001745565.1:n.1612G>A (CPA6)
NM_020361.5:c.804G>A (CPA6) MANE Select	NP_065094.3:p.Val268=