Canonical Allele Identifier: CA4214893

Gene: BMPER

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.33905729C>G , CM000669.2:g.33905729C>G	GRCh38
NC_000007.13:g.33945341C>G , CM000669.1:g.33945341C>G	GRCh37
NC_000007.12:g.33911866C>G	NCBI36
NG_031933.1:g.5819C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001365308.1:c.116C>G MANE Select	NP_001352237.1:p.Ala39Gly
ENST00000649409.2:c.116C>G MANE Select	ENSP00000497748.1:p.Ala39Gly
NM_133468.4:c.116C>G	NP_597725.1:p.Ala39Gly
NM_133468.5:c.116C>G	NP_597725.1:p.Ala39Gly
ENST00000297161.6:c.116C>G	ENSP00000297161.2:p.Ala39Gly
ENST00000436222.5:c.116C>G	ENSP00000399843.2:p.Ala39Gly
ENST00000436222.6:n.236-1089C>G
ENST00000444773.1:c.116C>G	ENSP00000409998.1:p.Ala39Gly
ENST00000448280.5:c.116C>G	ENSP00000398835.1:p.Ala39Gly
ENST00000496609.1:n.227C>G
ENST00000647656.1:c.116C>G	ENSP00000497346.1:p.Ala39Gly
ENST00000648229.1:c.116C>G	ENSP00000498201.1:p.Ala39Gly
ENST00000648305.1:c.116C>G	ENSP00000497365.1:p.Ala39Gly
ENST00000648392.1:c.116C>G	ENSP00000497488.1:p.Ala39Gly
ENST00000648445.1:c.116C>G	ENSP00000498008.1:p.Ala39Gly
ENST00000648618.1:c.116C>G	ENSP00000496953.1:p.Ala39Gly
ENST00000648848.1:c.116C>G	ENSP00000497963.1:p.Ala39Gly
ENST00000649002.1:c.116C>G	ENSP00000496926.1:p.Ala39Gly
ENST00000650206.1:c.116C>G	ENSP00000497637.1:p.Ala39Gly
ENST00000650350.1:c.59C>G	ENSP00000497933.1:p.Ala20Gly
ENST00000650544.1:c.116C>G	ENSP00000497982.1:p.Ala39Gly
XM_005249633.1:c.116C>G	XP_005249690.1:p.Ala39Gly
XM_005249633.3:c.116C>G	XP_005249690.1:p.Ala39Gly
XM_017011800.2:c.-439C>G	XP_016867289.1:n.-439C>G
XM_017011801.2:c.-439C>G	XP_016867290.1:n.-439C>G
XR_428072.1:n.230C>G