Canonical Allele Identifier: CA1790976418

Gene: CPA6

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67506804G= , CM000670.2:g.67506804G=	GRCh38
NC_000008.10:g.68419039G= , CM000670.1:g.68419039G=	GRCh37
NC_000008.9:g.68581593G=	NCBI36
NG_027682.1:g.244582C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020361.5:c.619C= MANE Select	NP_065094.3:p.Gln207=
ENST00000297770.10:c.619C= MANE Select	ENSP00000297770.4:p.Gln207=
NM_020361.4:c.619C=	NP_065094.3:p.Gln207=
ENST00000297770.8:c.619C=	ENSP00000297770.4:p.Gln207=
ENST00000479862.6:c.*215C=	ENSP00000419016.2:n.*215C=
ENST00000518549.1:c.619C=	ENSP00000431112.1:p.Gln207=
ENST00000638254.1:c.*215C=	ENSP00000491129.1:n.*215C=
XM_011517569.1:c.619C=	XP_011515871.1:p.Gln207=
XM_011517570.1:c.175C=	XP_011515872.1:p.Gln59=
XM_011517570.2:c.175C=	XP_011515872.1:p.Gln59=
XM_017013646.1:c.175C=	XP_016869135.1:p.Gln59=
XM_017013647.1:c.619C=	XP_016869136.1:p.Gln207=
XR_001745565.1:n.1427C=