Canonical Allele Identifier: CA371260810

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68396023T>G (hg19) ; chr8:g.67483788T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483788T>G , CM000670.2:g.67483788T>G	GRCh38
NC_000008.10:g.68396023T>G , CM000670.1:g.68396023T>G	GRCh37
NC_000008.9:g.68558577T>G	NCBI36
NG_027682.1:g.267598A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.818A>C (CPA6) MANE Select	ENSP00000297770.4:p.Asn273Thr
ENST00000638254.1:c.*414A>C (CPA6)	ENSP00000491129.1:n.*414A>C
ENST00000297770.8:c.818A>C (CPA6)	ENSP00000297770.4:p.Asn273Thr
ENST00000479862.6:c.*414A>C (CPA6)	ENSP00000419016.2:n.*414A>C
ENST00000518549.1:c.818A>C (CPA6)	ENSP00000431112.1:p.Asn273Thr
NM_020361.4:c.818A>C (CPA6)	NP_065094.3:p.Asn273Thr
XM_011517569.1:c.911A>C (CPA6)	XP_011515871.1:p.Asn304Thr
XM_011517570.1:c.374A>C (CPA6)	XP_011515872.1:p.Asn125Thr
NR_136224.1:n.694-7177T>G (ARFGEF1-DT)
XM_011517570.2:c.374A>C (CPA6)	XP_011515872.1:p.Asn125Thr
XM_017013646.1:c.374A>C (CPA6)	XP_016869135.1:p.Asn125Thr
XR_001745565.1:n.1626A>C (CPA6)
NM_020361.5:c.818A>C (CPA6) MANE Select	NP_065094.3:p.Asn273Thr