Canonical Allele Identifier: CA2370192051

Gene: BCAS1

Linked Data

• dbSNP Id: rs2276498

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.53993957C>A , CM000682.2:g.53993957C>A	GRCh38
NC_000020.10:g.52610496C>A , CM000682.1:g.52610496C>A	GRCh37
NC_000020.9:g.52043903C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000422805.2:c.66+1055G>T	ENSP00000399936.2:n.66+1055G>T
ENST00000685429.1:c.801+1055G>T	ENSP00000510480.1:n.801+1055G>T
ENST00000686565.1:c.927+1055G>T	ENSP00000509740.1:n.927+1055G>T
ENST00000688711.1:c.66+1055G>T	ENSP00000509228.1:n.66+1055G>T
ENST00000688948.1:c.927+1055G>T MANE Select	ENSP00000508731.1:n.927+1055G>T
ENST00000689476.1:c.66+1055G>T	ENSP00000509069.1:n.66+1055G>T
ENST00000690125.1:c.66+1055G>T	ENSP00000510030.1:n.66+1055G>T
ENST00000371435.6:c.927+1055G>T	ENSP00000360490.2:n.927+1055G>T
ENST00000371440.7:c.561+1055G>T	ENSP00000360495.4:n.561+1055G>T
ENST00000395961.7:c.927+1055G>T	ENSP00000379290.3:n.927+1055G>T
ENST00000422805.1:c.83+1055G>T
ENST00000448484.5:c.513+1055G>T	ENSP00000396361.1:n.513+1055G>T
NM_001316361.1:c.927+1055G>T	NP_001303290.1:n.927+1055G>T
NM_003657.2:c.927+1055G>T	NP_003648.2:n.927+1055G>T
XM_005260587.1:c.927+1055G>T	XP_005260644.1:n.927+1055G>T
XM_005260589.1:c.927+1055G>T	XP_005260646.1:n.927+1055G>T
XM_005260590.1:c.927+1055G>T	XP_005260647.1:n.927+1055G>T
XM_005260591.1:c.927+1055G>T	XP_005260648.1:n.927+1055G>T
XM_005260593.1:c.927+1055G>T	XP_005260650.1:n.927+1055G>T
XM_005260594.1:c.927+1055G>T	XP_005260651.1:n.927+1055G>T
XM_005260595.1:c.927+1055G>T	XP_005260652.1:n.927+1055G>T
XM_011529090.1:c.927+1055G>T	XP_011527392.1:n.927+1055G>T
XM_011529091.1:c.927+1055G>T	XP_011527393.1:n.927+1055G>T
NM_001316361.2:c.927+1055G>T	NP_001303290.1:n.927+1055G>T
NM_001323347.1:c.927+1055G>T	NP_001310276.1:n.927+1055G>T
NM_001366295.1:c.927+1055G>T	NP_001353224.1:n.927+1055G>T
NM_001366296.1:c.927+1055G>T	NP_001353225.1:n.927+1055G>T
NM_001366297.1:c.927+1055G>T	NP_001353226.1:n.927+1055G>T
NM_001366298.1:c.927+1055G>T	NP_001353227.1:n.927+1055G>T
NM_003657.3:c.927+1055G>T	NP_003648.2:n.927+1055G>T
XM_005260589.3:c.927+1055G>T	XP_005260646.1:n.927+1055G>T
XM_005260590.3:c.927+1055G>T	XP_005260647.1:n.927+1055G>T
XM_005260591.3:c.927+1055G>T	XP_005260648.1:n.927+1055G>T
XM_005260594.3:c.927+1055G>T	XP_005260651.1:n.927+1055G>T
XM_005260595.3:c.927+1055G>T	XP_005260652.1:n.927+1055G>T
XM_011529090.3:c.927+1055G>T	XP_011527392.1:n.927+1055G>T
XM_011529091.3:c.927+1055G>T	XP_011527393.1:n.927+1055G>T
XM_017028111.2:c.927+1055G>T	XP_016883600.1:n.927+1055G>T
NM_001316361.3:c.927+1055G>T	NP_001303290.1:n.927+1055G>T
NM_001323347.2:c.927+1055G>T	NP_001310276.1:n.927+1055G>T
NM_001366295.2:c.927+1055G>T	NP_001353224.1:n.927+1055G>T
NM_001366296.2:c.927+1055G>T	NP_001353225.1:n.927+1055G>T
NM_001366297.2:c.927+1055G>T	NP_001353226.1:n.927+1055G>T
NM_001366298.2:c.927+1055G>T MANE Select	NP_001353227.1:n.927+1055G>T
NM_003657.4:c.927+1055G>T	NP_003648.2:n.927+1055G>T