Canonical Allele Identifier: CA2623554645

Gene: PCCA

Linked Data

• gnomAD v4: 13-100089019-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100089019T>C , CM000675.2:g.100089019T>C	GRCh38
NC_000013.10:g.100741273T>C , CM000675.1:g.100741273T>C	GRCh37
NC_000013.9:g.99539274T>C	NCBI36
NG_008768.1:g.4937T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376279.7:c.-102T>C	ENSP00000365456.3:n.-102T>C
ENST00000376286.8:c.-102T>C	ENSP00000365463.4:n.-102T>C
NM_000282.3:c.-102T>C	NP_000273.2:n.-102T>C
NM_001127692.2:c.-102T>C	NP_001121164.1:n.-102T>C
NM_001178004.1:c.-102T>C	NP_001171475.1:n.-102T>C
NM_001352605.1:c.-102T>C	NP_001339534.1:n.-102T>C
NM_001352606.1:c.-102T>C	NP_001339535.1:n.-102T>C
NM_001352607.1:c.-102T>C	NP_001339536.1:n.-102T>C
NM_001352608.1:c.-102T>C	NP_001339537.1:n.-102T>C
NM_001352609.1:c.-102T>C	NP_001339538.1:n.-102T>C
NM_001352610.1:c.-968T>C	NP_001339539.1:n.-968T>C
NM_001352611.1:c.-968T>C	NP_001339540.1:n.-968T>C
NM_001352612.1:c.-968T>C	NP_001339541.1:n.-968T>C
NR_148027.1:n.5T>C
NR_148028.1:n.5T>C
NR_148029.1:n.5T>C
NR_148030.1:n.5T>C
NR_148031.1:n.5T>C