Canonical Allele Identifier: CA2639137572

Gene: BCAS3

Linked Data

• gnomAD v4: 17-61388244-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61388244T>G , CM000679.2:g.61388244T>G	GRCh38
NC_000017.10:g.59465605T>G , CM000679.1:g.59465605T>G	GRCh37
NC_000017.9:g.56820387T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000407086.8:c.2594-3733T>G MANE Select	ENSP00000385323.2:n.2594-3733T>G
ENST00000390652.9:c.2639-3733T>G	ENSP00000375067.4:n.2639-3733T>G
ENST00000407086.7:c.2594-3733T>G	ENSP00000385323.2:n.2594-3733T>G
ENST00000408905.7:c.2660-3733T>G	ENSP00000386173.2:n.2660-3733T>G
ENST00000585744.5:c.1952-3733T>G	ENSP00000468682.1:n.1952-3733T>G
ENST00000585812.5:n.1360-3733T>G
ENST00000587294.5:n.732-3733T>G
ENST00000588462.5:c.2705-3733T>G	ENSP00000468592.1:n.2705-3733T>G
ENST00000588569.1:n.488-374T>G
ENST00000588874.5:c.1907-3733T>G	ENSP00000464825.1:n.1907-3733T>G
ENST00000589222.5:c.2660-374T>G	ENSP00000466078.1:n.2660-374T>G
ENST00000592702.5:n.1240-3733T>G
NM_001099432.1:c.2639-3733T>G	NP_001092902.1:n.2639-3733T>G
NM_017679.3:c.2594-3733T>G	NP_060149.3:n.2594-3733T>G
XM_005257472.1:c.2705-3733T>G	XP_005257529.1:n.2705-3733T>G
XM_005257475.1:c.2660-374T>G	XP_005257532.1:n.2660-374T>G
XM_011524939.1:c.3074-3733T>G	XP_011523241.1:n.3074-3733T>G
XM_011524940.1:c.3029-3733T>G	XP_011523242.1:n.3029-3733T>G
XM_011524941.1:c.2939-3733T>G	XP_011523243.1:n.2939-3733T>G
XM_011524942.1:c.2795-3733T>G	XP_011523244.1:n.2795-3733T>G
XM_011524943.1:c.2750-3733T>G	XP_011523245.1:n.2750-3733T>G
XM_011524944.1:c.2729-3733T>G	XP_011523246.1:n.2729-3733T>G
XM_011524945.1:c.2684-3733T>G	XP_011523247.1:n.2684-3733T>G
XM_011524952.1:c.1907-3733T>G	XP_011523254.1:n.1907-3733T>G
NM_001099432.2:c.2639-3733T>G	NP_001092902.1:n.2639-3733T>G
NM_001320470.2:c.2660-374T>G	NP_001307399.1:n.2660-374T>G
NM_001330413.1:c.2705-3733T>G	NP_001317342.1:n.2705-3733T>G
NM_001330414.1:c.2660-3733T>G	NP_001317343.1:n.2660-3733T>G
NM_001353144.1:c.2729-3733T>G	NP_001340073.1:n.2729-3733T>G
NM_001353145.1:c.2684-3733T>G	NP_001340074.1:n.2684-3733T>G
NM_001353146.1:c.2639-374T>G	NP_001340075.1:n.2639-374T>G
NM_017679.4:c.2594-3733T>G	NP_060149.3:n.2594-3733T>G
XM_011524939.2:c.3074-3733T>G	XP_011523241.1:n.3074-3733T>G
XM_011524940.2:c.3029-3733T>G	XP_011523242.1:n.3029-3733T>G
XM_011524941.2:c.2939-3733T>G	XP_011523243.1:n.2939-3733T>G
XM_011524942.3:c.2795-3733T>G	XP_011523244.1:n.2795-3733T>G
XM_011524943.3:c.2750-3733T>G	XP_011523245.1:n.2750-3733T>G
XM_017024783.2:c.3074-374T>G	XP_016880272.1:n.3074-374T>G
XM_017024784.2:c.3008-3733T>G	XP_016880273.1:n.3008-3733T>G
XM_017024785.2:c.3008-374T>G	XP_016880274.1:n.3008-374T>G
XM_017024786.2:c.2984-3733T>G	XP_016880275.1:n.2984-3733T>G
XM_017024787.2:c.2936-3733T>G	XP_016880276.1:n.2936-3733T>G
XM_017024788.2:c.2870-3733T>G	XP_016880277.1:n.2870-3733T>G
XM_017024789.2:c.2729-374T>G	XP_016880278.1:n.2729-374T>G
XM_017024790.2:c.2705-374T>G	XP_016880279.1:n.2705-374T>G
XM_017024793.2:c.2594-374T>G	XP_016880282.1:n.2594-374T>G
XM_017024796.1:c.1952-3733T>G	XP_016880285.1:n.1952-3733T>G
XM_024450813.1:c.1907-3733T>G	XP_024306581.1:n.1907-3733T>G
NM_001099432.3:c.2639-3733T>G	NP_001092902.1:n.2639-3733T>G
NM_001320470.3:c.2660-374T>G	NP_001307399.1:n.2660-374T>G
NM_001330413.2:c.2705-3733T>G	NP_001317342.1:n.2705-3733T>G
NM_001330414.2:c.2660-3733T>G	NP_001317343.1:n.2660-3733T>G
NM_001353144.2:c.2729-3733T>G	NP_001340073.1:n.2729-3733T>G
NM_001353145.2:c.2684-3733T>G	NP_001340074.1:n.2684-3733T>G
NM_001353146.2:c.2639-374T>G	NP_001340075.1:n.2639-374T>G
NM_017679.5:c.2594-3733T>G MANE Select	NP_060149.3:n.2594-3733T>G