Canonical Allele Identifier: CA396797039

Gene: BCAR1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75251469A>G , CM000678.2:g.75251469A>G	GRCh38
NC_000016.9:g.75285367A>G , CM000678.1:g.75285367A>G	GRCh37
NC_000016.8:g.73842868A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014567.5:c.12+2T>C MANE Select	NP_055382.2:n.12+2T>C
ENST00000162330.10:c.12+2T>C MANE Select	ENSP00000162330.5:n.12+2T>C
NM_001170714.1:c.151-8379T>C	NP_001164185.1:n.151-8379T>C
NM_001170714.2:c.151-8379T>C	NP_001164185.1:n.151-8379T>C
NM_001170714.3:c.151-8379T>C	NP_001164185.1:n.151-8379T>C
NM_001170715.1:c.67-8379T>C	NP_001164186.1:n.67-8379T>C
NM_001170715.2:c.67-8379T>C	NP_001164186.1:n.67-8379T>C
NM_001170715.3:c.67-8379T>C	NP_001164186.1:n.67-8379T>C
NM_001170716.1:c.67-8379T>C	NP_001164187.1:n.67-8379T>C
NM_001170716.2:c.67-8379T>C	NP_001164187.1:n.67-8379T>C
NM_001170716.3:c.67-8379T>C	NP_001164187.1:n.67-8379T>C
NM_001170717.1:c.12+2T>C	NP_001164188.1:n.12+2T>C
NM_001170717.2:c.12+2T>C	NP_001164188.1:n.12+2T>C
NM_001170717.3:c.12+2T>C	NP_001164188.1:n.12+2T>C
NM_001170718.1:c.13-8379T>C	NP_001164189.1:n.13-8379T>C
NM_001170718.2:c.13-8379T>C	NP_001164189.1:n.13-8379T>C
NM_001170718.3:c.13-8379T>C	NP_001164189.1:n.13-8379T>C
NM_001170720.1:c.12+766T>C	NP_001164191.1:n.12+766T>C
NM_001170720.2:c.12+766T>C	NP_001164191.1:n.12+766T>C
NM_001170720.3:c.12+766T>C	NP_001164191.1:n.12+766T>C
NM_014567.3:c.12+2T>C	NP_055382.2:n.12+2T>C
NM_014567.4:c.12+2T>C	NP_055382.2:n.12+2T>C
ENST00000162330.9:c.12+2T>C	ENSP00000162330.5:n.12+2T>C
ENST00000393420.10:c.12+2T>C	ENSP00000377072.6:n.12+2T>C
ENST00000393422.6:c.67-8379T>C	ENSP00000377074.2:n.67-8379T>C
ENST00000418647.7:c.151-8379T>C	ENSP00000391669.3:n.151-8379T>C
ENST00000420641.7:c.67-8379T>C	ENSP00000392708.3:n.67-8379T>C
ENST00000535626.6:c.12+766T>C	ENSP00000440370.2:n.12+766T>C
ENST00000538440.6:c.13-8379T>C	ENSP00000443841.2:n.13-8379T>C
ENST00000562556.5:c.*690-8379T>C	ENSP00000455166.1:n.*690-8379T>C
ENST00000563323.1:c.-75-8379T>C	ENSP00000457097.1:n.-75-8379T>C
ENST00000564028.1:c.-76+330T>C	ENSP00000455810.1:n.-76+330T>C
ENST00000568864.1:c.-75-8379T>C	ENSP00000456625.1:n.-75-8379T>C
ENST00000569006.1:c.-76+4673T>C	ENSP00000458088.1:n.-76+4673T>C
XM_005256258.3:c.91-8379T>C	XP_005256315.1:n.91-8379T>C
XM_005256258.5:c.91-8379T>C	XP_005256315.1:n.91-8379T>C
XM_005256259.3:c.12+766T>C	XP_005256316.1:n.12+766T>C
XM_005256259.5:c.12+766T>C	XP_005256316.1:n.12+766T>C
XM_011523473.1:c.163-8379T>C	XP_011521775.1:n.163-8379T>C
XM_011523474.1:c.12+2T>C	XP_011521776.1:n.12+2T>C
XM_011523475.1:c.-75-8379T>C	XP_011521777.1:n.-75-8379T>C
XM_011523475.3:c.-75-8379T>C	XP_011521777.1:n.-75-8379T>C
XM_017023897.2:c.151-8379T>C	XP_016879386.1:n.151-8379T>C
XM_017023898.2:c.151-8379T>C	XP_016879387.1:n.151-8379T>C
XM_017023899.2:c.151-8379T>C	XP_016879388.1:n.151-8379T>C
XM_024450494.1:c.-75-8379T>C	XP_024306262.1:n.-75-8379T>C
XM_024450495.1:c.-87T>C	XP_024306263.1:n.-87T>C
XM_024450496.1:c.-76+443T>C	XP_024306264.1:n.-76+443T>C