Canonical Allele Identifier: CA388640977

Gene: PCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.100530097G>C , CM000675.2:g.100530097G>C	GRCh38
NC_000013.10:g.101182351G>C , CM000675.1:g.101182351G>C	GRCh37
NC_000013.9:g.99980352G>C	NCBI36
NG_008768.1:g.446015G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000282.4:c.2119-1G>C MANE Select	NP_000273.2:n.2119-1G>C
ENST00000376285.6:c.2119-1G>C MANE Select	ENSP00000365462.1:n.2119-1G>C
NM_000282.3:c.2119-1G>C	NP_000273.2:n.2119-1G>C
NM_001127692.2:c.2041-1G>C	NP_001121164.1:n.2041-1G>C
NM_001127692.3:c.2041-1G>C	NP_001121164.1:n.2041-1G>C
NM_001178004.1:c.1978-1G>C	NP_001171475.1:n.1978-1G>C
NM_001178004.2:c.1978-1G>C	NP_001171475.1:n.1978-1G>C
NM_001352605.1:c.2065-1G>C	NP_001339534.1:n.2065-1G>C
NM_001352605.2:c.2065-1G>C	NP_001339534.1:n.2065-1G>C
NM_001352606.1:c.1975-1G>C	NP_001339535.1:n.1975-1G>C
NM_001352606.2:c.1975-1G>C	NP_001339535.1:n.1975-1G>C
NM_001352607.1:c.1900-1G>C	NP_001339536.1:n.1900-1G>C
NM_001352607.2:c.1900-1G>C	NP_001339536.1:n.1900-1G>C
NM_001352608.1:c.1897-1G>C	NP_001339537.1:n.1897-1G>C
NM_001352608.2:c.1897-1G>C	NP_001339537.1:n.1897-1G>C
NM_001352610.1:c.1174-1G>C	NP_001339539.1:n.1174-1G>C
NM_001352610.2:c.1174-1G>C	NP_001339539.1:n.1174-1G>C
NM_001352611.1:c.1120-1G>C	NP_001339540.1:n.1120-1G>C
NM_001352611.2:c.1120-1G>C	NP_001339540.1:n.1120-1G>C
NM_001352612.1:c.1030-1G>C	NP_001339541.1:n.1030-1G>C
NM_001352612.2:c.1030-1G>C	NP_001339541.1:n.1030-1G>C
NR_148027.1:n.2168-1G>C
NR_148027.2:n.2090-1G>C
NR_148028.1:n.2206-1G>C
NR_148028.2:n.2128-1G>C
NR_148029.1:n.2128-1G>C
NR_148029.2:n.2050-1G>C
NR_148030.1:n.2309-1G>C
NR_148030.2:n.2231-1G>C
NR_148031.1:n.2122-1G>C
NR_148031.2:n.2044-1G>C
ENST00000376279.7:c.1978-1G>C	ENSP00000365456.3:n.1978-1G>C
ENST00000376285.5:c.2119-1G>C	ENSP00000365462.1:n.2119-1G>C
ENST00000376286.8:c.2041-1G>C	ENSP00000365463.4:n.2041-1G>C
ENST00000428969.1:c.268-1G>C	ENSP00000399413.1:n.268-1G>C
ENST00000458283.5:c.335-1G>C
ENST00000636366.1:c.1317-1G>C
ENST00000636475.1:c.1634-1G>C
ENST00000637657.1:c.1779-1G>C
ENST00000647303.1:c.*1603-1G>C	ENSP00000495663.1:n.*1603-1G>C
XM_017020609.1:c.2020-1G>C	XP_016876098.1:n.2020-1G>C
XM_017020613.1:c.*47-1G>C	XP_016876102.1:n.*47-1G>C
XR_001749567.1:n.2299-1G>C
XR_001749568.1:n.2386-1G>C
XR_001749569.1:n.2245-1G>C
XR_001749576.1:n.1856-1G>C
XR_001749577.1:n.1753-1G>C
XR_931615.1:n.1976-1G>C