Canonical Allele Identifier: CA236301
Community Standard Title: NM_020361.5(CPA6):c.544C>T (p.Arg182Ter)
Gene: CPA6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.67506879G>A , CM000670.2:g.67506879G>A GRCh38
NC_000008.10:g.68419114G>A , CM000670.1:g.68419114G>A GRCh37
NC_000008.9:g.68581668G>A NCBI36
NG_027682.1:g.244507C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020361.5:c.544C>T MANE Select NP_065094.3:p.Arg182Ter
ENST00000297770.10:c.544C>T MANE Select ENSP00000297770.4:p.Arg182Ter
NM_020361.4:c.544C>T NP_065094.3:p.Arg182Ter
ENST00000297770.8:c.544C>T ENSP00000297770.4:p.Arg182Ter
ENST00000479862.6:c.*140C>T ENSP00000419016.2:n.*140C>T
ENST00000518549.1:c.544C>T ENSP00000431112.1:p.Arg182Ter
ENST00000638254.1:c.*140C>T ENSP00000491129.1:n.*140C>T
XM_011517569.1:c.544C>T XP_011515871.1:p.Arg182Ter
XM_011517570.1:c.100C>T XP_011515872.1:p.Arg34Ter
XM_011517570.2:c.100C>T XP_011515872.1:p.Arg34Ter
XM_017013646.1:c.100C>T XP_016869135.1:p.Arg34Ter
XM_017013647.1:c.544C>T XP_016869136.1:p.Arg182Ter
XR_001745565.1:n.1352C>T