Canonical Allele Identifier: CA354647156

Gene: PCCB

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136316939A>C , CM000665.2:g.136316939A>C	GRCh38
NC_000003.11:g.136035781A>C , CM000665.1:g.136035781A>C	GRCh37
NC_000003.10:g.137518471A>C	NCBI36
NG_008939.1:g.71615A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000532.5:c.967-2A>C MANE Select	NP_000523.2:n.967-2A>C
ENST00000251654.9:c.967-2A>C MANE Select	ENSP00000251654.4:n.967-2A>C
NM_000532.4:c.967-2A>C	NP_000523.2:n.967-2A>C
NM_001178014.1:c.1027-2A>C	NP_001171485.1:n.1027-2A>C
NM_001178014.2:c.1027-2A>C	NP_001171485.1:n.1027-2A>C
ENST00000251654.8:c.967-2A>C	ENSP00000251654.4:n.967-2A>C
ENST00000462637.5:c.898-2A>C	ENSP00000420391.1:n.898-2A>C
ENST00000466072.5:c.967-2A>C	ENSP00000420158.1:n.967-2A>C
ENST00000468777.5:c.1060-2A>C	ENSP00000419129.1:n.1060-2A>C
ENST00000469217.5:c.1027-2A>C	ENSP00000419027.1:n.1027-2A>C
ENST00000471595.5:c.967-2A>C	ENSP00000417549.1:n.967-2A>C
ENST00000473073.1:n.924-2A>C
ENST00000474833.5:n.592-2A>C
ENST00000475214.5:n.881-2A>C
ENST00000478469.5:c.885-17341A>C	ENSP00000420759.1:n.885-17341A>C
ENST00000482086.5:c.619-2A>C	ENSP00000417253.1:n.619-2A>C
ENST00000483687.5:c.910-2A>C	ENSP00000420639.1:n.910-2A>C
ENST00000484181.5:c.967-2A>C	ENSP00000417937.1:n.967-2A>C
ENST00000490504.5:c.796-2A>C	ENSP00000418307.1:n.796-2A>C
XM_011512873.1:c.967-2A>C	XP_011511175.1:n.967-2A>C
XM_011512873.2:c.967-2A>C	XP_011511175.1:n.967-2A>C