Canonical Allele Identifier: CA14390341
Gene: BAIAP2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs7502931

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81044877A>G , CM000679.2:g.81044877A>G GRCh38
NC_000017.10:g.79018677A>G , CM000679.1:g.79018677A>G GRCh37
NC_000017.9:g.76633272A>G NCBI36
NG_029486.1:g.14731A>G
NG_029486.2:g.14731A>G

Transcript Alleles

HGVS Amino-acid change
NM_001144888.1:c.55-8791A>G VV NP_001138360.1:p.=
NM_006340.2:c.55-8791A>G VV NP_006331.1:p.=
NM_017450.2:c.55-8791A>G VV NP_059344.1:p.=
NM_017451.2:c.55-8791A>G VV NP_059345.1:p.=
XM_005256943.1:c.153+7916A>G XP_005257000.1:p.=
XM_005256944.1:c.153+7916A>G XP_005257001.1:p.=
XM_005256945.1:c.153+7916A>G XP_005257002.1:p.=
XM_005256948.2:c.55-8791A>G XP_005257005.1:p.=
XM_006721635.1:c.153+7916A>G XP_006721698.1:p.=
XM_006721636.1:c.153+7916A>G XP_006721699.1:p.=
XM_006721637.1:c.55-8791A>G XP_006721700.1:p.=
XM_011524193.1:c.153+7916A>G XP_011522495.1:p.=
XM_011524194.1:c.153+7916A>G XP_011522496.1:p.=
XM_005256948.3:c.55-8791A>G XP_005257005.1:p.=
XM_006721637.2:c.55-8791A>G XP_006721700.1:p.=
XM_024450534.1:c.-703-8791A>G XP_024306302.1:p.=
ENST00000321280.11:c.55-8791A>G ENSP00000315685.7:p.=
ENST00000321300.10:c.55-8791A>G ENSP00000316338.6:p.=
ENST00000428708.6:c.55-8791A>G ENSP00000401022.2:p.=
ENST00000435091.7:c.55-8791A>G ENSP00000413069.3:p.=
ENST00000570913.5:n.159-8791A>G
ENST00000571530.5:c.-7+7916A>G ENSP00000458202.1:p.=
ENST00000572329.5:c.153+7916A>G ENSP00000460492.1:p.=
ENST00000573894.5:n.134-8791A>G
ENST00000575245.5:c.153+7916A>G ENSP00000461144.1:p.=
ENST00000575712.5:c.55-8791A>G ENSP00000458964.1:p.=
ENST00000575750.5:c.55-8791A>G ENSP00000460344.1:p.=
ENST00000575989.5:c.-168-8791A>G ENSP00000458494.1:p.=
ENST00000576470.5:n.162-8791A>G