Canonical Allele Identifier: CA371260712

Gene: CPA6 ARFGEF1-DT

Linked Data

• MyVariant Identifiers: chr8:g.68395984C>A (hg19) ; chr8:g.67483749C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483749C>A , CM000670.2:g.67483749C>A	GRCh38
NC_000008.10:g.68395984C>A , CM000670.1:g.68395984C>A	GRCh37
NC_000008.9:g.68558538C>A	NCBI36
NG_027682.1:g.267637G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.838+19G>T (CPA6) MANE Select	ENSP00000297770.4:n.838+19G>T
ENST00000638254.1:c.*434+19G>T (CPA6)	ENSP00000491129.1:n.*434+19G>T
ENST00000297770.8:c.838+19G>T (CPA6)	ENSP00000297770.4:n.838+19G>T
ENST00000479862.6:c.*434+19G>T (CPA6)	ENSP00000419016.2:n.*434+19G>T
ENST00000518549.1:c.857G>T (CPA6)	ENSP00000431112.1:p.Trp286Leu
NM_020361.4:c.838+19G>T (CPA6)	NP_065094.3:n.838+19G>T
XM_011517569.1:c.931+19G>T (CPA6)	XP_011515871.1:n.931+19G>T
XM_011517570.1:c.394+19G>T (CPA6)	XP_011515872.1:n.394+19G>T
NR_136224.1:n.694-7216C>A (ARFGEF1-DT)
XM_011517570.2:c.394+19G>T (CPA6)	XP_011515872.1:n.394+19G>T
XM_017013646.1:c.394+19G>T (CPA6)	XP_016869135.1:n.394+19G>T
XR_001745565.1:n.1646+19G>T (CPA6)
NM_020361.5:c.838+19G>T (CPA6) MANE Select	NP_065094.3:n.838+19G>T