Canonical Allele Identifier: CA2632153

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136327686C>T , CM000665.2:g.136327686C>T	GRCh38
NC_000003.11:g.136046528C>T , CM000665.1:g.136046528C>T	GRCh37
NC_000003.10:g.137529218C>T	NCBI36
NG_008939.1:g.82362C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.1352C>T MANE Select	NP_000523.2:p.Thr451Ile
ENST00000251654.9:c.1352C>T MANE Select	ENSP00000251654.4:p.Thr451Ile
NM_000532.4:c.1352C>T	NP_000523.2:p.Thr451Ile
NM_001178014.1:c.1412C>T	NP_001171485.1:p.Thr471Ile
NM_001178014.2:c.1412C>T	NP_001171485.1:p.Thr471Ile
ENST00000251654.8:c.1352C>T	ENSP00000251654.4:p.Thr451Ile
ENST00000462637.5:c.1283C>T	ENSP00000420391.1:p.Thr428Ile
ENST00000466072.5:c.1412C>T	ENSP00000420158.1:p.Thr471Ile
ENST00000468777.5:c.1445C>T	ENSP00000419129.1:p.Thr482Ile
ENST00000469217.5:c.1412C>T	ENSP00000419027.1:p.Thr471Ile
ENST00000471595.5:c.1352C>T	ENSP00000417549.1:p.Thr451Ile
ENST00000473073.1:n.1553C>T
ENST00000474833.5:n.876C>T
ENST00000478469.5:c.885-6594C>T	ENSP00000420759.1:n.885-6594C>T
ENST00000482086.5:c.1004C>T	ENSP00000417253.1:p.Thr335Ile
ENST00000483687.5:c.1295C>T	ENSP00000420639.1:p.Thr432Ile
ENST00000484181.5:c.*33C>T	ENSP00000417937.1:n.*33C>T
ENST00000490504.5:c.1181C>T	ENSP00000418307.1:p.Thr394Ile