Canonical Allele Identifier: CA371260689

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68395974A>C (hg19) ; chr8:g.67483739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483739A>C , CM000670.2:g.67483739A>C	GRCh38
NC_000008.10:g.68395974A>C , CM000670.1:g.68395974A>C	GRCh37
NC_000008.9:g.68558528A>C	NCBI36
NG_027682.1:g.267647T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.838+29T>G (CPA6) MANE Select	ENSP00000297770.4:n.838+29T>G
ENST00000638254.1:c.*434+29T>G (CPA6)	ENSP00000491129.1:n.*434+29T>G
ENST00000297770.8:c.838+29T>G (CPA6)	ENSP00000297770.4:n.838+29T>G
ENST00000479862.6:c.*434+29T>G (CPA6)	ENSP00000419016.2:n.*434+29T>G
ENST00000518549.1:c.867T>G (CPA6)	ENSP00000431112.1:p.Asp289Glu
NM_020361.4:c.838+29T>G (CPA6)	NP_065094.3:n.838+29T>G
XM_011517569.1:c.931+29T>G (CPA6)	XP_011515871.1:n.931+29T>G
XM_011517570.1:c.394+29T>G (CPA6)	XP_011515872.1:n.394+29T>G
NR_136224.1:n.694-7226A>C (ARFGEF1-DT)
XM_011517570.2:c.394+29T>G (CPA6)	XP_011515872.1:n.394+29T>G
XM_017013646.1:c.394+29T>G (CPA6)	XP_016869135.1:n.394+29T>G
XR_001745565.1:n.1646+29T>G (CPA6)
NM_020361.5:c.838+29T>G (CPA6) MANE Select	NP_065094.3:n.838+29T>G