Canonical Allele Identifier: CA1743216801

Gene: CPA5

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.130363698_130363700delinsTTG , CM000669.2:g.130363698_130363700delinsTTG	GRCh38
NC_000007.13:g.130003539_130003541delinsTTG , CM000669.1:g.130003539_130003541delinsTTG	GRCh37
NC_000007.12:g.129790775_129790777delinsTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474905.6:c.838+189_838+191delinsTTG MANE Select	ENSP00000417314.1:n.838+189_838+191delinsTTG
ENST00000393213.7:c.838+189_838+191delinsTTG	ENSP00000376907.3:n.838+189_838+191delinsTTG
ENST00000431780.6:c.838+189_838+191delinsTTG	ENSP00000393045.2:n.838+189_838+191delinsTTG
ENST00000461828.5:c.838+189_838+191delinsTTG	ENSP00000418183.1:n.838+189_838+191delinsTTG
ENST00000466363.6:c.838+189_838+191delinsTTG	ENSP00000419025.2:n.838+189_838+191delinsTTG
ENST00000474905.5:c.838+189_838+191delinsTTG	ENSP00000417314.1:n.838+189_838+191delinsTTG
ENST00000479492.1:c.69+189_69+191delinsTTG
ENST00000485477.5:c.838+189_838+191delinsTTG	ENSP00000420237.1:n.838+189_838+191delinsTTG
ENST00000495736.1:n.1060+189_1060+191delinsTTG
NM_001127441.1:c.838+189_838+191delinsTTG	NP_001120913.1:n.838+189_838+191delinsTTG
NM_001127442.1:c.838+189_838+191delinsTTG	NP_001120914.1:n.838+189_838+191delinsTTG
NM_080385.4:c.838+189_838+191delinsTTG	NP_525124.3:n.838+189_838+191delinsTTG
XM_005250710.1:c.838+189_838+191delinsTTG	XP_005250767.1:n.838+189_838+191delinsTTG
XM_005250711.1:c.838+189_838+191delinsTTG	XP_005250768.1:n.838+189_838+191delinsTTG
XM_005250712.1:c.838+189_838+191delinsTTG	XP_005250769.1:n.838+189_838+191delinsTTG
XM_011516698.1:c.838+189_838+191delinsTTG	XP_011515000.1:n.838+189_838+191delinsTTG
XM_011516699.1:c.838+189_838+191delinsTTG	XP_011515001.1:n.838+189_838+191delinsTTG
XM_011516700.1:c.838+189_838+191delinsTTG	XP_011515002.1:n.838+189_838+191delinsTTG
XM_011516701.1:c.838+189_838+191delinsTTG	XP_011515003.1:n.838+189_838+191delinsTTG
XM_011516702.1:c.838+189_838+191delinsTTG	XP_011515004.1:n.838+189_838+191delinsTTG
XM_011516703.1:c.838+189_838+191delinsTTG	XP_011515005.1:n.838+189_838+191delinsTTG
XM_011516704.1:c.838+189_838+191delinsTTG	XP_011515006.1:n.838+189_838+191delinsTTG
XM_011516705.1:c.838+189_838+191delinsTTG	XP_011515007.1:n.838+189_838+191delinsTTG
XR_927548.1:n.2037+189_2037+191delinsTTG
XR_927549.1:n.2037+189_2037+191delinsTTG
XR_927550.1:n.2037+189_2037+191delinsTTG
XR_927551.1:n.2037+189_2037+191delinsTTG
NM_001318223.1:c.838+189_838+191delinsTTG	NP_001305152.1:n.838+189_838+191delinsTTG
XM_024446999.1:c.838+189_838+191delinsTTG	XP_024302767.1:n.838+189_838+191delinsTTG
XM_024447000.1:c.838+189_838+191delinsTTG	XP_024302768.1:n.838+189_838+191delinsTTG
XM_024447001.1:c.838+189_838+191delinsTTG	XP_024302769.1:n.838+189_838+191delinsTTG
NM_001127441.2:c.838+189_838+191delinsTTG	NP_001120913.1:n.838+189_838+191delinsTTG
NM_001127442.2:c.838+189_838+191delinsTTG	NP_001120914.1:n.838+189_838+191delinsTTG
NM_001318223.2:c.838+189_838+191delinsTTG	NP_001305152.1:n.838+189_838+191delinsTTG
NM_080385.5:c.838+189_838+191delinsTTG MANE Select	NP_525124.3:n.838+189_838+191delinsTTG