Canonical Allele Identifier: CA1404303722

Gene: PCCB

Linked Data

• dbSNP Id: rs1935349572

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327149_136327150insA , CM000665.2:g.136327149_136327150insA	GRCh38
NC_000003.11:g.136045991_136045992insA , CM000665.1:g.136045991_136045992insA	GRCh37
NC_000003.10:g.137528681_137528682insA	NCBI36
NG_008939.1:g.81825_81826insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000251654.9:c.1199-6_1199-5insA MANE Select	ENSP00000251654.4:n.1199-6_1199-5insA
ENST00000251654.8:c.1199-6_1199-5insA	ENSP00000251654.4:n.1199-6_1199-5insA
ENST00000462637.5:c.1130-6_1130-5insA	ENSP00000420391.1:n.1130-6_1130-5insA
ENST00000466072.5:c.1259-6_1259-5insA	ENSP00000420158.1:n.1259-6_1259-5insA
ENST00000468777.5:c.1292-6_1292-5insA	ENSP00000419129.1:n.1292-6_1292-5insA
ENST00000469217.5:c.1259-6_1259-5insA	ENSP00000419027.1:n.1259-6_1259-5insA
ENST00000471595.5:c.1199-6_1199-5insA	ENSP00000417549.1:n.1199-6_1199-5insA
ENST00000473073.1:n.1394_1395insA
ENST00000474833.5:n.823+239_823+240insA
ENST00000478469.5:c.885-7131_885-7130insA	ENSP00000420759.1:n.885-7131_885-7130insA...
ENST00000482086.5:c.851-6_851-5insA	ENSP00000417253.1:n.851-6_851-5insA
ENST00000483687.5:c.1142-6_1142-5insA	ENSP00000420639.1:n.1142-6_1142-5insA
ENST00000484181.5:c.1198+239_1198+240insA	ENSP00000417937.1:n.1198+239_1198+240insA...
ENST00000490504.5:c.1028-6_1028-5insA	ENSP00000418307.1:n.1028-6_1028-5insA
NM_000532.4:c.1199-6_1199-5insA	NP_000523.2:n.1199-6_1199-5insA
NM_001178014.1:c.1259-6_1259-5insA	NP_001171485.1:n.1259-6_1259-5insA
NM_000532.5:c.1199-6_1199-5insA MANE Select	NP_000523.2:n.1199-6_1199-5insA
NM_001178014.2:c.1259-6_1259-5insA	NP_001171485.1:n.1259-6_1259-5insA