Canonical Allele Identifier: CA10161252
Community Standard Title: NM_032608.7(MYO18B):c.5697C>T (p.Asp1899=)
Gene: MYO18B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.25947777C>T , CM000684.2:g.25947777C>T GRCh38
NC_000022.10:g.26343743C>T , CM000684.1:g.26343743C>T GRCh37
NC_000022.9:g.24673743C>T NCBI36
NG_046772.1:g.210634C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032608.7:c.5697C>T MANE Select NP_115997.5:p.Asp1899=
ENST00000335473.12:c.5697C>T MANE Select ENSP00000334563.8:p.Asp1899=
NM_001318245.1:c.5700C>T NP_001305174.1:p.Asp1900=
NM_001318245.2:c.5700C>T NP_001305174.1:p.Asp1900=
NM_032608.5:c.5697C>T NP_115997.5:p.Asp1899=
NM_032608.6:c.5697C>T NP_115997.5:p.Asp1899=
ENST00000335473.11:c.5697C>T ENSP00000334563.7:p.Asp1899=
ENST00000407587.6:c.5700C>T ENSP00000386096.2:p.Asp1900=
ENST00000418374.6:n.4268C>T
ENST00000536101.5:c.5697C>T ENSP00000441229.1:p.Asp1899=
ENST00000539302.5:c.*3155C>T ENSP00000437587.1:n.*3155C>T
XM_005261786.3:c.5700C>T XP_005261843.1:p.Asp1900=
XM_011530458.1:c.5826C>T XP_011528760.1:p.Asp1942=
XM_011530458.2:c.5826C>T XP_011528760.1:p.Asp1942=
XM_011530459.1:c.5826C>T XP_011528761.1:p.Asp1942=
XM_011530459.2:c.5826C>T XP_011528761.1:p.Asp1942=
XM_011530460.1:c.5826C>T XP_011528762.1:p.Asp1942=
XM_011530460.2:c.5826C>T XP_011528762.1:p.Asp1942=
XM_011530461.1:c.5826C>T XP_011528763.1:p.Asp1942=
XM_011530461.2:c.5826C>T XP_011528763.1:p.Asp1942=
XM_011530462.1:c.5826C>T XP_011528764.1:p.Asp1942=
XM_011530463.1:c.5826C>T XP_011528765.1:p.Asp1942=
XM_011530464.1:c.5823C>T XP_011528766.1:p.Asp1941=
XM_011530464.2:c.5823C>T XP_011528766.1:p.Asp1941=
XM_011530465.1:c.5343C>T XP_011528767.1:p.Asp1781=
XM_011530465.2:c.5343C>T XP_011528767.1:p.Asp1781=
XM_011530466.1:c.5826C>T XP_011528768.1:p.Asp1942=
XM_011530466.2:c.5826C>T XP_011528768.1:p.Asp1942=
XM_017029012.1:c.5826C>T XP_016884501.1:p.Asp1942=
XM_017029013.1:c.5826C>T XP_016884502.1:p.Asp1942=
XM_017029014.1:c.5823C>T XP_016884503.1:p.Asp1941=
XM_017029015.1:c.5694C>T XP_016884504.1:p.Asp1898=
XM_017029016.1:c.3162C>T XP_016884505.1:p.Asp1054=
XM_017029017.1:c.3159C>T XP_016884506.1:p.Asp1053=