Canonical Allele Identifier: CA1699040130
Gene: BMPER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.34054385A>T , CM000669.2:g.34054385A>T GRCh38
NC_000007.13:g.34093997A>T , CM000669.1:g.34093997A>T GRCh37
NC_000007.12:g.34060522A>T NCBI36
NG_031933.1:g.154475A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647656.1:c.*189-778A>T ENSP00000497346.1:n.*189-778A>T
ENST00000647703.1:n.287-778A>T
ENST00000648229.1:c.687-778A>T ENSP00000498201.1:n.687-778A>T
ENST00000648305.1:c.577-24472A>T ENSP00000497365.1:n.577-24472A>T
ENST00000648320.1:n.240-778A>T
ENST00000648392.1:c.787-778A>T ENSP00000497488.1:n.787-778A>T
ENST00000648445.1:c.787-778A>T ENSP00000498008.1:n.787-778A>T
ENST00000648618.1:c.*189-778A>T ENSP00000496953.1:n.*189-778A>T
ENST00000648848.1:c.787-778A>T ENSP00000497963.1:n.787-778A>T
ENST00000648856.1:c.583-778A>T ENSP00000496854.1:n.583-778A>T
ENST00000648982.1:c.380-778A>T
ENST00000649002.1:c.687-778A>T ENSP00000496926.1:n.687-778A>T
ENST00000649232.1:c.618-778A>T ENSP00000497721.1:n.618-778A>T
ENST00000649409.2:c.787-778A>T MANE Select ENSP00000497748.1:n.787-778A>T
ENST00000649771.1:c.583-778A>T ENSP00000497314.1:n.583-778A>T
ENST00000649985.1:c.*142-778A>T ENSP00000497578.1:n.*142-778A>T
ENST00000650202.1:c.*189-778A>T ENSP00000497972.1:n.*189-778A>T
ENST00000650206.1:c.*92-778A>T ENSP00000497637.1:n.*92-778A>T
ENST00000650350.1:c.530-778A>T ENSP00000497933.1:n.530-778A>T
ENST00000650533.1:c.483-778A>T ENSP00000497081.1:n.483-778A>T
ENST00000650544.1:c.787-778A>T ENSP00000497982.1:n.787-778A>T
ENST00000297161.6:c.787-778A>T ENSP00000297161.2:n.787-778A>T
ENST00000494786.1:n.505-778A>T
NM_133468.4:c.787-778A>T NP_597725.1:n.787-778A>T
XM_005249633.1:c.787-778A>T XP_005249690.1:n.787-778A>T
XR_428072.1:n.901-778A>T
NM_001365308.1:c.787-778A>T MANE Select NP_001352237.1:n.787-778A>T
NM_133468.5:c.787-778A>T NP_597725.1:n.787-778A>T
XM_005249633.3:c.787-778A>T XP_005249690.1:n.787-778A>T
XM_017011800.2:c.133-778A>T XP_016867289.1:n.133-778A>T
XM_017011801.2:c.133-778A>T XP_016867290.1:n.133-778A>T