Canonical Allele Identifier: CA15966926

Gene: BCL2L1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.31718172A>G , CM000682.2:g.31718172A>G	GRCh38
NC_000020.10:g.30305975A>G , CM000682.1:g.30305975A>G	GRCh37
NC_000020.9:g.29769636A>G	NCBI36
NG_029002.1:g.9682T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307677.5:c.564+3483T>C MANE Select	ENSP00000302564.4:n.564+3483T>C
ENST00000376055.9:c.375+3672T>C	ENSP00000365223.4:n.375+3672T>C
ENST00000420488.6:c.564+3483T>C	ENSP00000390760.2:n.564+3483T>C
ENST00000422920.2:c.375+3672T>C	ENSP00000411252.2:n.375+3672T>C
ENST00000434194.2:c.564+3483T>C	ENSP00000401173.2:n.564+3483T>C
ENST00000439267.2:c.564+3483T>C	ENSP00000389688.2:n.564+3483T>C
ENST00000450273.2:c.564+3483T>C	ENSP00000406203.2:n.564+3483T>C
ENST00000456404.6:c.564+3483T>C	ENSP00000395545.2:n.564+3483T>C
ENST00000676582.1:c.564+3483T>C	ENSP00000503725.1:n.564+3483T>C
ENST00000676942.1:c.564+3483T>C	ENSP00000504536.1:n.564+3483T>C
ENST00000677194.1:c.564+3483T>C	ENSP00000504387.1:n.564+3483T>C
ENST00000677494.1:n.73+1173T>C
ENST00000678563.1:c.564+3483T>C	ENSP00000504237.1:n.564+3483T>C
ENST00000678671.1:c.564+3483T>C	ENSP00000504137.1:n.564+3483T>C
ENST00000307677.4:c.564+3483T>C	ENSP00000302564.4:n.564+3483T>C
ENST00000376055.8:c.375+3672T>C	ENSP00000365223.4:n.375+3672T>C
ENST00000376062.6:c.564+3483T>C	ENSP00000365230.2:n.564+3483T>C
ENST00000450273.1:c.564+3483T>C	ENSP00000406203.1:n.564+3483T>C
NM_001191.2:c.375+3672T>C	NP_001182.1:n.375+3672T>C
NM_138578.1:c.564+3483T>C	NP_612815.1:n.564+3483T>C
XM_005260486.2:c.564+3483T>C	XP_005260543.1:n.564+3483T>C
XM_005260487.3:c.564+3483T>C	XP_005260544.1:n.564+3483T>C
XM_011528960.1:c.564+3483T>C	XP_011527262.1:n.564+3483T>C
XM_011528961.1:c.564+3483T>C	XP_011527263.1:n.564+3483T>C
XM_011528962.1:c.564+3483T>C	XP_011527264.1:n.564+3483T>C
XM_011528963.1:c.564+3483T>C	XP_011527265.1:n.564+3483T>C
XM_011528964.1:c.564+3483T>C	XP_011527266.1:n.564+3483T>C
XM_011528965.1:c.564+3483T>C	XP_011527267.1:n.564+3483T>C
XM_011528966.1:c.564+3483T>C	XP_011527268.1:n.564+3483T>C
XR_936599.1:n.942+3483T>C
NM_001191.3:c.375+3672T>C	NP_001182.1:n.375+3672T>C
NM_001317919.1:c.564+3483T>C	NP_001304848.1:n.564+3483T>C
NM_001317920.1:c.564+3483T>C	NP_001304849.1:n.564+3483T>C
NM_001317921.1:c.564+3483T>C	NP_001304850.1:n.564+3483T>C
NM_001322239.1:c.564+3483T>C	NP_001309168.1:n.564+3483T>C
NM_001322240.1:c.564+3483T>C	NP_001309169.1:n.564+3483T>C
NM_001322242.1:c.564+3483T>C	NP_001309171.1:n.564+3483T>C
NM_138578.2:c.564+3483T>C	NP_612815.1:n.564+3483T>C
NR_134257.1:n.676+3483T>C
XM_011528964.2:c.564+3483T>C	XP_011527266.1:n.564+3483T>C
XM_017027993.1:c.564+3483T>C	XP_016883482.1:n.564+3483T>C
XR_001754364.2:n.927+3483T>C
XR_936599.3:n.945+3483T>C
NM_138578.3:c.564+3483T>C MANE Select	NP_612815.1:n.564+3483T>C
NM_001191.4:c.375+3672T>C	NP_001182.1:n.375+3672T>C
NM_001317919.2:c.564+3483T>C	NP_001304848.1:n.564+3483T>C
NM_001317920.2:c.564+3483T>C	NP_001304849.1:n.564+3483T>C
NM_001317921.2:c.564+3483T>C	NP_001304850.1:n.564+3483T>C
NM_001322239.2:c.564+3483T>C	NP_001309168.1:n.564+3483T>C
NM_001322240.2:c.564+3483T>C	NP_001309169.1:n.564+3483T>C
NM_001322242.2:c.564+3483T>C	NP_001309171.1:n.564+3483T>C