Canonical Allele Identifier: CA1883830907
Gene: SOHLH1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.135699350_135699351delinsCT , CM000671.2:g.135699350_135699351delinsCT GRCh38
NC_000009.11:g.138591196_138591197delinsCT , CM000671.1:g.138591196_138591197delinsCT GRCh37
NC_000009.10:g.137731017_137731018delinsCT NCBI36
NG_033070.1:g.2166_2167delinsCT
NG_033784.1:g.5178_5179delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000425225.2:c.65+52_65+53delinsAG MANE Select ENSP00000404438.1:n.65+52_65+53delinsAG
ENST00000674066.1:n.1217-225_1217-224delinsAG
ENST00000298466.9:c.65+52_65+53delinsAG ENSP00000298466.5:n.65+52_65+53delinsAG
ENST00000425225.1:c.65+52_65+53delinsAG ENSP00000404438.1:n.65+52_65+53delinsAG
NM_001012415.2:c.65+52_65+53delinsAG NP_001012415.2:n.65+52_65+53delinsAG
NM_001101677.1:c.65+52_65+53delinsAG NP_001095147.1:n.65+52_65+53delinsAG
XM_005263403.2:c.65+52_65+53delinsAG XP_005263460.1:n.65+52_65+53delinsAG
XM_006717109.2:c.-139-225_-139-224delinsAG XP_006717172.1:n.-139-225_-139-224delinsAG
XM_011518698.1:c.65+52_65+53delinsAG XP_011517000.1:n.65+52_65+53delinsAG
XM_005263403.3:c.65+52_65+53delinsAG XP_005263460.1:n.65+52_65+53delinsAG
XM_006717109.4:c.-139-225_-139-224delinsAG XP_006717172.1:n.-139-225_-139-224delinsAG
XM_011518698.3:c.65+52_65+53delinsAG XP_011517000.1:n.65+52_65+53delinsAG
XM_024447552.1:c.-139-225_-139-224delinsAG XP_024303320.1:n.-139-225_-139-224delinsAG
NM_001012415.3:c.65+52_65+53delinsAG NP_001012415.3:n.65+52_65+53delinsAG
NM_001101677.2:c.65+52_65+53delinsAG MANE Select NP_001095147.2:n.65+52_65+53delinsAG