Canonical Allele Identifier: CA2838196324

Gene: BCAR3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.93584692C>A , CM000663.2:g.93584692C>A	GRCh38
NC_000001.10:g.94050249C>A , CM000663.1:g.94050249C>A	GRCh37
NC_000001.9:g.93822837C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260502.11:c.930-571G>T MANE Select	ENSP00000260502.6:n.930-571G>T
ENST00000260502.10:c.930-571G>T	ENSP00000260502.6:n.930-571G>T
ENST00000370243.1:c.930-571G>T	ENSP00000359263.1:n.930-571G>T
ENST00000370244.5:c.930-571G>T	ENSP00000359264.1:n.930-571G>T
ENST00000370247.7:c.657-571G>T	ENSP00000359267.3:n.657-571G>T
ENST00000466632.1:n.130+280G>T
ENST00000539242.5:c.-44+280G>T	ENSP00000441343.1:n.-44+280G>T
NM_001261408.1:c.930-571G>T	NP_001248337.1:n.930-571G>T
NM_001261409.1:c.930-571G>T	NP_001248338.1:n.930-571G>T
NM_001261410.1:c.657-571G>T	NP_001248339.1:n.657-571G>T
NM_001308251.1:c.-44+280G>T	NP_001295180.1:n.-44+280G>T
NM_003567.3:c.930-571G>T	NP_003558.1:n.930-571G>T
XM_011542251.1:c.270-571G>T	XP_011540553.1:n.270-571G>T
XM_017002480.1:c.930-571G>T	XP_016857969.1:n.930-571G>T
NM_003567.4:c.930-571G>T MANE Select	NP_003558.1:n.930-571G>T
NM_001261408.2:c.930-571G>T	NP_001248337.1:n.930-571G>T
NM_001261410.2:c.657-571G>T	NP_001248339.1:n.657-571G>T