Canonical Allele Identifier: CA2580577070
Gene: BCAS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.61379228C>A , CM000679.2:g.61379228C>A GRCh38
NC_000017.10:g.59456589C>A , CM000679.1:g.59456589C>A GRCh37
NC_000017.9:g.56811371C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000407086.8:c.2593+10734C>A MANE Select ENSP00000385323.2:n.2593+10734C>A
ENST00000390652.9:c.2638+10734C>A ENSP00000375067.4:n.2638+10734C>A
ENST00000407086.7:c.2593+10734C>A ENSP00000385323.2:n.2593+10734C>A
ENST00000408905.7:c.2594-1278C>A ENSP00000386173.2:n.2594-1278C>A
ENST00000585744.5:c.1951+10734C>A ENSP00000468682.1:n.1951+10734C>A
ENST00000585812.5:n.1293+88C>A
ENST00000587294.5:n.666-1278C>A
ENST00000587872.1:n.1399C>A
ENST00000588462.5:c.2639-1278C>A ENSP00000468592.1:n.2639-1278C>A
ENST00000588569.1:n.422-1278C>A
ENST00000588874.5:c.1906+10734C>A ENSP00000464825.1:n.1906+10734C>A
ENST00000589222.5:c.2594-1278C>A ENSP00000466078.1:n.2594-1278C>A
ENST00000592702.5:n.1239+10734C>A
NM_001099432.1:c.2638+10734C>A NP_001092902.1:n.2638+10734C>A
NM_017679.3:c.2593+10734C>A NP_060149.3:n.2593+10734C>A
XM_005257472.1:c.2639-1278C>A XP_005257529.1:n.2639-1278C>A
XM_005257475.1:c.2594-1278C>A XP_005257532.1:n.2594-1278C>A
XM_011524939.1:c.3008-1278C>A XP_011523241.1:n.3008-1278C>A
XM_011524940.1:c.2963-1278C>A XP_011523242.1:n.2963-1278C>A
XM_011524941.1:c.2873-1278C>A XP_011523243.1:n.2873-1278C>A
XM_011524942.1:c.2729-1278C>A XP_011523244.1:n.2729-1278C>A
XM_011524943.1:c.2684-1278C>A XP_011523245.1:n.2684-1278C>A
XM_011524944.1:c.2728+10734C>A XP_011523246.1:n.2728+10734C>A
XM_011524945.1:c.2683+10734C>A XP_011523247.1:n.2683+10734C>A
XM_011524952.1:c.1906+10734C>A XP_011523254.1:n.1906+10734C>A
XM_011525568.1:c.-29+3984G>T XP_011523870.1:n.-29+3984G>T
NM_001099432.2:c.2638+10734C>A NP_001092902.1:n.2638+10734C>A
NM_001320470.2:c.2594-1278C>A NP_001307399.1:n.2594-1278C>A
NM_001330413.1:c.2639-1278C>A NP_001317342.1:n.2639-1278C>A
NM_001330414.1:c.2594-1278C>A NP_001317343.1:n.2594-1278C>A
NM_001353144.1:c.2728+10734C>A NP_001340073.1:n.2728+10734C>A
NM_001353145.1:c.2683+10734C>A NP_001340074.1:n.2683+10734C>A
NM_001353146.1:c.2639-9390C>A NP_001340075.1:n.2639-9390C>A
NM_017679.4:c.2593+10734C>A NP_060149.3:n.2593+10734C>A
XM_011524939.2:c.3008-1278C>A XP_011523241.1:n.3008-1278C>A
XM_011524940.2:c.2963-1278C>A XP_011523242.1:n.2963-1278C>A
XM_011524941.2:c.2873-1278C>A XP_011523243.1:n.2873-1278C>A
XM_011524942.3:c.2729-1278C>A XP_011523244.1:n.2729-1278C>A
XM_011524943.3:c.2684-1278C>A XP_011523245.1:n.2684-1278C>A
XM_017024783.2:c.3008-1278C>A XP_016880272.1:n.3008-1278C>A
XM_017024784.2:c.3007+10734C>A XP_016880273.1:n.3007+10734C>A
XM_017024785.2:c.3008-9390C>A XP_016880274.1:n.3008-9390C>A
XM_017024786.2:c.2918-1278C>A XP_016880275.1:n.2918-1278C>A
XM_017024787.2:c.2870-1278C>A XP_016880276.1:n.2870-1278C>A
XM_017024788.2:c.2869+10734C>A XP_016880277.1:n.2869+10734C>A
XM_017024789.2:c.2729-9390C>A XP_016880278.1:n.2729-9390C>A
XM_017024790.2:c.2639-1278C>A XP_016880279.1:n.2639-1278C>A
XM_017024793.2:c.2594-9390C>A XP_016880282.1:n.2594-9390C>A
XM_017024796.1:c.1951+10734C>A XP_016880285.1:n.1951+10734C>A
XM_024450813.1:c.1906+10734C>A XP_024306581.1:n.1906+10734C>A
NM_001099432.3:c.2638+10734C>A NP_001092902.1:n.2638+10734C>A
NM_001320470.3:c.2594-1278C>A NP_001307399.1:n.2594-1278C>A
NM_001330413.2:c.2639-1278C>A NP_001317342.1:n.2639-1278C>A
NM_001330414.2:c.2594-1278C>A NP_001317343.1:n.2594-1278C>A
NM_001353144.2:c.2728+10734C>A NP_001340073.1:n.2728+10734C>A
NM_001353145.2:c.2683+10734C>A NP_001340074.1:n.2683+10734C>A
NM_001353146.2:c.2639-9390C>A NP_001340075.1:n.2639-9390C>A
NM_017679.5:c.2593+10734C>A MANE Select NP_060149.3:n.2593+10734C>A
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