Canonical Allele Identifier: CA371260920
Gene: CPA6 HGNC NCBI
ARFGEF1-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.67483842T>A , CM000670.2:g.67483842T>A GRCh38
NC_000008.10:g.68396077T>A , CM000670.1:g.68396077T>A GRCh37
NC_000008.9:g.68558631T>A NCBI36
NG_027682.1:g.267544A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297770.10:c.764A>T (CPA6) MANE Select ENSP00000297770.4:p.Lys255Ile
ENST00000638254.1:c.*360A>T (CPA6) ENSP00000491129.1:n.*360A>T
ENST00000297770.8:c.764A>T (CPA6) ENSP00000297770.4:p.Lys255Ile
ENST00000479862.6:c.*360A>T (CPA6) ENSP00000419016.2:n.*360A>T
ENST00000518549.1:c.764A>T (CPA6) ENSP00000431112.1:p.Lys255Ile
NM_020361.4:c.764A>T (CPA6) NP_065094.3:p.Lys255Ile
XM_011517569.1:c.857A>T (CPA6) XP_011515871.1:p.Lys286Ile
XM_011517570.1:c.320A>T (CPA6) XP_011515872.1:p.Lys107Ile
NR_136224.1:n.694-7123T>A (ARFGEF1-DT)
XM_011517570.2:c.320A>T (CPA6) XP_011515872.1:p.Lys107Ile
XM_017013646.1:c.320A>T (CPA6) XP_016869135.1:p.Lys107Ile
XR_001745565.1:n.1572A>T (CPA6)
NM_020361.5:c.764A>T (CPA6) MANE Select NP_065094.3:p.Lys255Ile