Canonical Allele Identifier: CA1364885841
Gene: STAB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52498003G= , CM000665.2:g.52498003G= GRCh38
NC_000003.11:g.52532019G= , CM000665.1:g.52532019G= GRCh37
NC_000003.10:g.52507059G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000321725.10:c.78+2512G= MANE Select ENSP00000312946.6:n.78+2512G=
ENST00000479355.1:n.123+2512G=
ENST00000481607.1:n.133+2512G=
NM_015136.2:c.78+2512G= NP_055951.2:n.78+2512G=
XM_005264973.2:c.78+2512G= XP_005265030.1:n.78+2512G=
XM_005264974.2:c.78+2512G= XP_005265031.1:n.78+2512G=
XM_005264975.2:c.78+2512G= XP_005265032.1:n.78+2512G=
XM_006713065.1:c.78+2512G= XP_006713128.1:n.78+2512G=
XM_011533528.1:c.78+2512G= XP_011531830.1:n.78+2512G=
XR_940395.1:n.154+2512G=
XM_005264973.3:c.78+2512G= XP_005265030.1:n.78+2512G=
XM_017005998.1:c.78+2512G= XP_016861487.1:n.78+2512G=
XM_017005999.1:c.78+2512G= XP_016861488.1:n.78+2512G=
XM_017006000.1:c.78+2512G= XP_016861489.1:n.78+2512G=
XM_017006001.1:c.78+2512G= XP_016861490.1:n.78+2512G=
XM_017006002.1:c.78+2512G= XP_016861491.1:n.78+2512G=
XM_017006003.1:c.78+2512G= XP_016861492.1:n.78+2512G=
XM_017006004.2:c.78+2512G= XP_016861493.1:n.78+2512G=
XR_001740064.1:n.154+2512G=
NM_015136.3:c.78+2512G= MANE Select NP_055951.2:n.78+2512G=