Canonical Allele Identifier: CA371260890

Gene: CPA6 ARFGEF1-DT

Linked Data

• gnomAD v4: 8-67483827-T-C
• MyVariant Identifiers: chr8:g.68396062T>C (hg19) ; chr8:g.67483827T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.67483827T>C , CM000670.2:g.67483827T>C	GRCh38
NC_000008.10:g.68396062T>C , CM000670.1:g.68396062T>C	GRCh37
NC_000008.9:g.68558616T>C	NCBI36
NG_027682.1:g.267559A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297770.10:c.779A>G (CPA6) MANE Select	ENSP00000297770.4:p.Asn260Ser
ENST00000638254.1:c.*375A>G (CPA6)	ENSP00000491129.1:n.*375A>G
ENST00000297770.8:c.779A>G (CPA6)	ENSP00000297770.4:p.Asn260Ser
ENST00000479862.6:c.*375A>G (CPA6)	ENSP00000419016.2:n.*375A>G
ENST00000518549.1:c.779A>G (CPA6)	ENSP00000431112.1:p.Asn260Ser
NM_020361.4:c.779A>G (CPA6)	NP_065094.3:p.Asn260Ser
XM_011517569.1:c.872A>G (CPA6)	XP_011515871.1:p.Asn291Ser
XM_011517570.1:c.335A>G (CPA6)	XP_011515872.1:p.Asn112Ser
NR_136224.1:n.694-7138T>C (ARFGEF1-DT)
XM_011517570.2:c.335A>G (CPA6)	XP_011515872.1:p.Asn112Ser
XM_017013646.1:c.335A>G (CPA6)	XP_016869135.1:p.Asn112Ser
XR_001745565.1:n.1587A>G (CPA6)
NM_020361.5:c.779A>G (CPA6) MANE Select	NP_065094.3:p.Asn260Ser