Canonical Allele Identifier: CA2695212663
Gene: SHOC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.110964877_110964878delinsAT , CM000672.2:g.110964877_110964878delinsAT GRCh38
NC_000010.10:g.112724635_112724636delinsAT , CM000672.1:g.112724635_112724636delinsAT GRCh37
NC_000010.9:g.112714625_112714626delinsAT NCBI36
NG_028922.1:g.50335_50336delinsAT , LRG_753:g.50335_50336delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000265277.10:c.519_520delinsAT ENSP00000265277.5:p.Met173_Leu174delinsIl...
ENST00000451838.2:c.-242-35538_-242-35537delinsAT ENSP00000408275.2:n.-242-35538_-242-35537...
ENST00000480155.2:n.755_756delinsAT
ENST00000685059.1:c.519_520delinsAT ENSP00000510210.1:p.Met173_Leu174delinsIl...
ENST00000685613.1:c.519_520delinsAT ENSP00000510564.1:p.Met173_Leu174delinsIl...
ENST00000687592.1:n.818_819delinsAT
ENST00000688928.1:c.519_520delinsAT ENSP00000509273.1:p.Met173_Leu174delinsIl...
ENST00000689118.1:c.519_520delinsAT ENSP00000510554.1:p.Met173_Leu174delinsIl...
ENST00000689300.1:c.519_520delinsAT ENSP00000510639.1:p.Met173_Leu174delinsIl...
ENST00000689997.1:c.-380-20751_-380-20750delinsAT ENSP00000510700.1:n.-380-20751_-380-20750...
ENST00000691151.1:n.811_812delinsAT
ENST00000691369.1:c.519_520delinsAT ENSP00000509754.1:p.Met173_Leu174delinsIl...
ENST00000691441.1:c.519_520delinsAT ENSP00000509686.1:p.Met173_Leu174delinsIl...
ENST00000691903.1:c.519_520delinsAT ENSP00000510314.1:p.Met173_Leu174delinsIl...
ENST00000692776.1:c.519_520delinsAT ENSP00000508524.1:p.Met173_Leu174delinsIl...
ENST00000369452.9:c.519_520delinsAT MANE Select ENSP00000358464.5:p.Met173_Leu174delinsIl...
ENST00000265277.9:c.519_520delinsAT ENSP00000265277.5:p.Met173_Leu174delinsIl...
ENST00000369452.8:c.519_520delinsAT ENSP00000358464.4:p.Met173_Leu174delinsIl...
ENST00000451838.1:c.27_28delinsAT ENSP00000408275.1:p.Met9_Leu10delinsIlePh...
ENST00000489390.1:n.56-35538_56-35537delinsAT
NM_001269039.1:c.519_520delinsAT NP_001255968.1:p.Met173_Leu174delinsIlePh...
NM_007373.3:c.519_520delinsAT , LRG_753t1:c.519_520delinsAT NP_031399.2:p.Met173_Leu174delinsIlePhe
XM_011540216.1:c.-380-20751_-380-20750delinsAT XP_011538518.1:n.-380-20751_-380-20750del...
NM_001269039.2:c.519_520delinsAT NP_001255968.1:p.Met173_Leu174delinsIlePh...
NM_001324336.1:c.519_520delinsAT NP_001311265.1:p.Met173_Leu174delinsIlePh...
NM_001324337.1:c.519_520delinsAT NP_001311266.1:p.Met173_Leu174delinsIlePh...
NR_136749.1:n.116-20751_116-20750delinsAT
NM_007373.4:c.519_520delinsAT MANE Select NP_031399.2:p.Met173_Leu174delinsIlePhe
NM_001269039.3:c.519_520delinsAT NP_001255968.1:p.Met173_Leu174delinsIlePh...
NM_001324336.2:c.519_520delinsAT NP_001311265.1:p.Met173_Leu174delinsIlePh...
NM_001324337.2:c.519_520delinsAT NP_001311266.1:p.Met173_Leu174delinsIlePh...
NR_136749.2:n.55-20751_55-20750delinsAT