Canonical Allele Identifier: CA454471492

Gene: BMPER

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.34061965dup , CM000669.2:g.34061965dup	GRCh38
NC_000007.13:g.34101577dup , CM000669.1:g.34101577dup	GRCh37
NC_000007.12:g.34068102dup	NCBI36
NG_031933.1:g.162055dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001365308.1:c.1033-37dup MANE Select	NP_001352237.1:n.1033-37dup
ENST00000649409.2:c.1033-37dup MANE Select	ENSP00000497748.1:n.1033-37dup
NM_133468.4:c.1033-37dup	NP_597725.1:n.1033-37dup
NM_133468.5:c.1033-37dup	NP_597725.1:n.1033-37dup
ENST00000297161.6:c.1033-37dup	ENSP00000297161.2:n.1033-37dup
ENST00000647656.1:c.*435-37dup	ENSP00000497346.1:n.*435-37dup
ENST00000647703.1:n.428-37dup
ENST00000648229.1:c.*57-37dup	ENSP00000498201.1:n.*57-37dup
ENST00000648305.1:c.577-16892dup	ENSP00000497365.1:n.577-16892dup
ENST00000648320.1:n.380+6662dup
ENST00000648392.1:c.927+6662dup	ENSP00000497488.1:n.927+6662dup
ENST00000648445.1:c.1032+3802dup	ENSP00000498008.1:n.1032+3802dup
ENST00000648618.1:c.*435-37dup	ENSP00000496953.1:n.*435-37dup
ENST00000648848.1:c.1033-37dup	ENSP00000497963.1:n.1033-37dup
ENST00000648856.1:c.829-37dup	ENSP00000496854.1:n.829-37dup
ENST00000648982.1:c.626-37dup
ENST00000649002.1:c.827+6662dup	ENSP00000496926.1:n.827+6662dup
ENST00000649232.1:c.864-37dup	ENSP00000497721.1:n.864-37dup
ENST00000649771.1:c.829-37dup	ENSP00000497314.1:n.829-37dup
ENST00000649985.1:c.*388-37dup	ENSP00000497578.1:n.*388-37dup
ENST00000650202.1:c.*435-37dup	ENSP00000497972.1:n.*435-37dup
ENST00000650206.1:c.*337+3802dup	ENSP00000497637.1:n.*337+3802dup
ENST00000650350.1:c.776-37dup	ENSP00000497933.1:n.776-37dup
ENST00000650533.1:c.*57-37dup	ENSP00000497081.1:n.*57-37dup
ENST00000650544.1:c.928-37dup	ENSP00000497982.1:n.928-37dup
XM_005249633.1:c.1033-37dup	XP_005249690.1:n.1033-37dup
XM_005249633.3:c.1033-37dup	XP_005249690.1:n.1033-37dup
XM_017011800.2:c.379-37dup	XP_016867289.1:n.379-37dup
XM_017011801.2:c.379-37dup	XP_016867290.1:n.379-37dup
XR_428072.1:n.1147-37dup