Canonical Allele Identifier: CA16296612

Gene: BMPER

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.34143063C>T , CM000669.2:g.34143063C>T	GRCh38
NC_000007.13:g.34182675C>T , CM000669.1:g.34182675C>T	GRCh37
NC_000007.12:g.34149200C>T	NCBI36
NG_031933.1:g.243153C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476525.2:n.408-167C>T
ENST00000647656.1:c.*1148-10029C>T	ENSP00000497346.1:n.*1148-10029C>T
ENST00000647703.1:n.1141-167C>T
ENST00000648229.1:c.*642-167C>T	ENSP00000498201.1:n.*642-167C>T
ENST00000648305.1:c.*575-167C>T	ENSP00000497365.1:n.*575-167C>T
ENST00000648320.1:n.1048-167C>T
ENST00000648392.1:c.1467-167C>T	ENSP00000497488.1:n.1467-167C>T
ENST00000648445.1:c.1572-167C>T	ENSP00000498008.1:n.1572-167C>T
ENST00000648618.1:c.*1148-167C>T	ENSP00000496953.1:n.*1148-167C>T
ENST00000648848.1:c.1416-167C>T	ENSP00000497963.1:n.1416-167C>T
ENST00000648856.1:c.1542-10029C>T	ENSP00000496854.1:n.1542-10029C>T
ENST00000648982.1:c.1339-167C>T
ENST00000649002.1:c.*619-167C>T	ENSP00000496926.1:n.*619-167C>T
ENST00000649232.1:c.1577-167C>T	ENSP00000497721.1:n.1577-167C>T
ENST00000649409.2:c.1746-167C>T MANE Select	ENSP00000497748.1:n.1746-167C>T
ENST00000649771.1:c.*235-167C>T	ENSP00000497314.1:n.*235-167C>T
ENST00000649985.1:c.*1101-167C>T	ENSP00000497578.1:n.*1101-167C>T
ENST00000650202.1:c.*1148-167C>T	ENSP00000497972.1:n.*1148-167C>T
ENST00000650206.1:c.*877-167C>T	ENSP00000497637.1:n.*877-167C>T
ENST00000650350.1:c.1489-167C>T	ENSP00000497933.1:n.1489-167C>T
ENST00000650533.1:c.*440-167C>T	ENSP00000497081.1:n.*440-167C>T
ENST00000650544.1:c.1641-167C>T	ENSP00000497982.1:n.1641-167C>T
ENST00000297161.6:c.1746-167C>T	ENSP00000297161.2:n.1746-167C>T
ENST00000476525.1:n.408-167C>T
NM_133468.4:c.1746-167C>T	NP_597725.1:n.1746-167C>T
XM_005249633.1:c.1416-167C>T	XP_005249690.1:n.1416-167C>T
XR_428072.1:n.1732-167C>T
NM_001365308.1:c.1746-167C>T MANE Select	NP_001352237.1:n.1746-167C>T
NM_133468.5:c.1746-167C>T	NP_597725.1:n.1746-167C>T
XM_005249633.3:c.1416-167C>T	XP_005249690.1:n.1416-167C>T
XM_017011800.2:c.1092-167C>T	XP_016867289.1:n.1092-167C>T
XM_017011801.2:c.762-167C>T	XP_016867290.1:n.762-167C>T