Canonical Allele Identifier: CA388967968

Gene: PABPN1 BCL2L2-PABPN1

Linked Data

• ClinVar Variation Id: 2434546
• ClinVar RCV Id: RCV003134724
• dbSNP Id: rs912588128
• gnomAD v2: 14-23790920-C-G
• gnomAD v3: 14-23321711-C-G
• gnomAD v4: 14-23321711-C-G
• MyVariant Identifiers: chr14:g.23790920C>G (hg19) ; chr14:g.23321711C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23321711C>G , CM000676.2:g.23321711C>G	GRCh38
NC_000014.8:g.23790920C>G , CM000676.1:g.23790920C>G	GRCh37
NC_000014.7:g.22860760C>G	NCBI36
NG_008239.1:g.6524C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216727.9:c.242C>G (PABPN1) MANE Select	ENSP00000216727.4:p.Pro81Arg
ENST00000678502.1:c.529-470C>G (BCL2L2-PABPN1)	ENSP00000503309.1:n.529-470C>G
ENST00000216727.8:c.242C>G (PABPN1)	ENSP00000216727.4:p.Pro81Arg
ENST00000397276.6:c.242C>G (PABPN1)	ENSP00000380446.2:p.Pro81Arg
ENST00000553781.5:c.433-470C>G (BCL2L2-PABPN1)	ENSP00000451320.1:n.433-470C>G
ENST00000556821.5:c.-503C>G (PABPN1)	ENSP00000451970.1:n.-503C>G
ENST00000557008.2:c.433-470C>G (BCL2L2-PABPN1)	ENSP00000452479.1:n.433-470C>G
NM_001199864.1:c.433-470C>G (BCL2L2-PABPN1)	NP_001186793.1:n.433-470C>G
NM_004643.3:c.242C>G (PABPN1)	NP_004634.1:p.Pro81Arg
NM_001360551.1:c.242C>G (PABPN1)	NP_001347480.1:p.Pro81Arg
NM_001199864.2:c.433-470C>G (BCL2L2-PABPN1)	NP_001186793.2:n.433-470C>G
NM_001360551.2:c.242C>G (PABPN1)	NP_001347480.1:p.Pro81Arg
NM_001199864.3:c.433-470C>G (BCL2L2-PABPN1)	NP_001186793.2:n.433-470C>G
NM_001360551.3:c.242C>G (PABPN1)	NP_001347480.1:p.Pro81Arg
NM_001387340.1:c.550-470C>G (BCL2L2-PABPN1)	NP_001374269.1:n.550-470C>G
NM_001387341.1:c.529-470C>G (BCL2L2-PABPN1)	NP_001374270.1:n.529-470C>G
NM_001387342.1:c.529-470C>G (BCL2L2-PABPN1)	NP_001374271.1:n.529-470C>G
NM_001387343.1:c.529-470C>G (BCL2L2-PABPN1)	NP_001374272.1:n.529-470C>G
NM_001387344.1:c.529-470C>G (BCL2L2-PABPN1)	NP_001374273.1:n.529-470C>G
NM_001387345.1:c.433-470C>G (BCL2L2-PABPN1)	NP_001374274.1:n.433-470C>G
NM_001387346.1:c.433-470C>G (BCL2L2-PABPN1)	NP_001374275.1:n.433-470C>G
NM_004643.4:c.242C>G (PABPN1) MANE Select	NP_004634.1:p.Pro81Arg