Canonical Allele Identifier: CA1743216904

Gene: CPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.130363799_130363800delinsTC , CM000669.2:g.130363799_130363800delinsTC	GRCh38
NC_000007.13:g.130003640_130003641delinsTC , CM000669.1:g.130003640_130003641delinsTC	GRCh37
NC_000007.12:g.129790876_129790877delinsTC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474905.6:c.838+290_838+291delinsTC MANE Select	ENSP00000417314.1:n.838+290_838+291delinsTC
ENST00000393213.7:c.838+290_838+291delinsTC	ENSP00000376907.3:n.838+290_838+291delinsTC
ENST00000431780.6:c.838+290_838+291delinsTC	ENSP00000393045.2:n.838+290_838+291delinsTC
ENST00000461828.5:c.838+290_838+291delinsTC	ENSP00000418183.1:n.838+290_838+291delinsTC
ENST00000466363.6:c.838+290_838+291delinsTC	ENSP00000419025.2:n.838+290_838+291delinsTC
ENST00000474905.5:c.838+290_838+291delinsTC	ENSP00000417314.1:n.838+290_838+291delinsTC
ENST00000479492.1:c.69+290_69+291delinsTC
ENST00000485477.5:c.838+290_838+291delinsTC	ENSP00000420237.1:n.838+290_838+291delinsTC
ENST00000495736.1:n.1060+290_1060+291delinsTC
NM_001127441.1:c.838+290_838+291delinsTC	NP_001120913.1:n.838+290_838+291delinsTC
NM_001127442.1:c.838+290_838+291delinsTC	NP_001120914.1:n.838+290_838+291delinsTC
NM_080385.4:c.838+290_838+291delinsTC	NP_525124.3:n.838+290_838+291delinsTC
XM_005250710.1:c.838+290_838+291delinsTC	XP_005250767.1:n.838+290_838+291delinsTC
XM_005250711.1:c.838+290_838+291delinsTC	XP_005250768.1:n.838+290_838+291delinsTC
XM_005250712.1:c.838+290_838+291delinsTC	XP_005250769.1:n.838+290_838+291delinsTC
XM_011516698.1:c.838+290_838+291delinsTC	XP_011515000.1:n.838+290_838+291delinsTC
XM_011516699.1:c.838+290_838+291delinsTC	XP_011515001.1:n.838+290_838+291delinsTC
XM_011516700.1:c.838+290_838+291delinsTC	XP_011515002.1:n.838+290_838+291delinsTC
XM_011516701.1:c.838+290_838+291delinsTC	XP_011515003.1:n.838+290_838+291delinsTC
XM_011516702.1:c.838+290_838+291delinsTC	XP_011515004.1:n.838+290_838+291delinsTC
XM_011516703.1:c.838+290_838+291delinsTC	XP_011515005.1:n.838+290_838+291delinsTC
XM_011516704.1:c.838+290_838+291delinsTC	XP_011515006.1:n.838+290_838+291delinsTC
XM_011516705.1:c.838+290_838+291delinsTC	XP_011515007.1:n.838+290_838+291delinsTC
XR_927548.1:n.2037+290_2037+291delinsTC
XR_927549.1:n.2037+290_2037+291delinsTC
XR_927550.1:n.2037+290_2037+291delinsTC
XR_927551.1:n.2037+290_2037+291delinsTC
NM_001318223.1:c.838+290_838+291delinsTC	NP_001305152.1:n.838+290_838+291delinsTC
XM_024446999.1:c.838+290_838+291delinsTC	XP_024302767.1:n.838+290_838+291delinsTC
XM_024447000.1:c.838+290_838+291delinsTC	XP_024302768.1:n.838+290_838+291delinsTC
XM_024447001.1:c.838+290_838+291delinsTC	XP_024302769.1:n.838+290_838+291delinsTC
NM_001127441.2:c.838+290_838+291delinsTC	NP_001120913.1:n.838+290_838+291delinsTC
NM_001127442.2:c.838+290_838+291delinsTC	NP_001120914.1:n.838+290_838+291delinsTC
NM_001318223.2:c.838+290_838+291delinsTC	NP_001305152.1:n.838+290_838+291delinsTC
NM_080385.5:c.838+290_838+291delinsTC MANE Select	NP_525124.3:n.838+290_838+291delinsTC