Canonical Allele Identifier: CA2144950947
Community Standard Title: NM_001034852.3(SMOC1):c.99+854A=
Gene: SMOC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.69880631A= , CM000676.2:g.69880631A= GRCh38
NC_000014.8:g.70347348A= , CM000676.1:g.70347348A= GRCh37
NC_000014.7:g.69417101A= NCBI36
NG_028217.1:g.6235A=

Transcript Alleles

HGVS Amino-acid Change
NM_001034852.3:c.99+854A= MANE Select NP_001030024.1:n.99+854A=
ENST00000361956.8:c.99+854A= MANE Select ENSP00000355110.4:n.99+854A=
NM_001034852.2:c.99+854A= NP_001030024.1:n.99+854A=
NM_022137.5:c.99+854A= NP_071420.1:n.99+854A=
NM_022137.6:c.99+854A= NP_071420.1:n.99+854A=
ENST00000361956.7:c.99+854A= ENSP00000355110.3:n.99+854A=
ENST00000381280.4:c.99+854A= ENSP00000370680.4:n.99+854A=
ENST00000555917.1:n.404+16417A=
XM_005267995.1:c.99+854A= XP_005268052.1:n.99+854A=
XM_005267996.1:c.99+854A= XP_005268053.1:n.99+854A=