Canonical Allele Identifier: CA2322264928

Gene: PPAN PPAN-P2RY11

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10107354C>G , CM000681.2:g.10107354C>G	GRCh38
NC_000019.9:g.10218030C>G , CM000681.1:g.10218030C>G	GRCh37
NC_000019.8:g.10079030C>G	NCBI36
NG_047007.1:g.834C>G
NG_051640.1:g.6132C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253107.12:c.190-151C>G (PPAN) MANE Select	ENSP00000253107.7:n.190-151C>G
ENST00000253107.11:c.190-151C>G (PPAN)	ENSP00000253107.7:n.190-151C>G
ENST00000393793.5:c.31-151C>G (PPAN)	ENSP00000377382.1:n.31-151C>G
ENST00000393796.4:c.190-151C>G (PPAN-P2RY11)	ENSP00000377385.4:n.190-151C>G
ENST00000428358.5:c.190-151C>G (PPAN-P2RY11)	ENSP00000411918.1:n.190-151C>G
ENST00000430370.1:c.4-151C>G (PPAN)	ENSP00000415988.1:n.4-151C>G
ENST00000446223.5:c.4-151C>G (PPAN)	ENSP00000410485.1:n.4-151C>G
NM_001040664.2:c.190-151C>G (PPAN-P2RY11)	NP_001035754.1:n.190-151C>G
NM_001198690.1:c.190-151C>G (PPAN-P2RY11)	NP_001185619.1:n.190-151C>G
NM_020230.5:c.190-151C>G (PPAN)	NP_064615.3:n.190-151C>G
NM_001346139.1:c.190-151C>G (PPAN)	NP_001333068.1:n.190-151C>G
NM_001346141.1:c.31-151C>G (PPAN)	NP_001333070.1:n.31-151C>G
NM_020230.6:c.190-151C>G (PPAN)	NP_064615.3:n.190-151C>G
NM_020230.7:c.190-151C>G (PPAN) MANE Select	NP_064615.3:n.190-151C>G
NM_001040664.3:c.190-151C>G (PPAN-P2RY11)	NP_001035754.1:n.190-151C>G
NM_001198690.2:c.190-151C>G (PPAN-P2RY11)	NP_001185619.1:n.190-151C>G