Canonical Allele Identifier: CA2610905980

Gene: SHOC2

Linked Data

• gnomAD v4: 10-110964327-TTCATGTAGTTTTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.110964330_110964343del , CM000672.2:g.110964330_110964343del	GRCh38
NC_000010.10:g.112724088_112724101del , CM000672.1:g.112724088_112724101del	GRCh37
NC_000010.9:g.112714078_112714091del	NCBI36
NG_028922.1:g.49788_49801del , LRG_753:g.49788_49801del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265277.10:c.-29_-16del	ENSP00000265277.5:n.-29_-16del
ENST00000451838.2:c.-242-36085_-242-36072del	ENSP00000408275.2:n.-242-36085_-242-36072del
ENST00000480155.2:n.208_221del
ENST00000685059.1:c.-29_-16del	ENSP00000510210.1:n.-29_-16del
ENST00000685613.1:c.-29_-16del	ENSP00000510564.1:n.-29_-16del
ENST00000687592.1:n.271_284del
ENST00000688928.1:c.-29_-16del	ENSP00000509273.1:n.-29_-16del
ENST00000689118.1:c.-29_-16del	ENSP00000510554.1:n.-29_-16del
ENST00000689300.1:c.-29_-16del	ENSP00000510639.1:n.-29_-16del
ENST00000689997.1:c.-380-21298_-380-21285del	ENSP00000510700.1:n.-380-21298_-380-21285del
ENST00000691151.1:n.264_277del
ENST00000691369.1:c.-29_-16del	ENSP00000509754.1:n.-29_-16del
ENST00000691441.1:c.-29_-16del	ENSP00000509686.1:n.-29_-16del
ENST00000691903.1:c.-29_-16del	ENSP00000510314.1:n.-29_-16del
ENST00000692776.1:c.-29_-16del	ENSP00000508524.1:n.-29_-16del
ENST00000369452.9:c.-29_-16del MANE Select	ENSP00000358464.5:n.-29_-16del
ENST00000265277.9:c.-29_-16del	ENSP00000265277.5:n.-29_-16del
ENST00000369452.8:c.-29_-16del	ENSP00000358464.4:n.-29_-16del
ENST00000480155.1:n.456_469del
ENST00000489390.1:n.56-36085_56-36072del
ENST00000489783.1:n.350_363del
NM_001269039.1:c.-29_-16del	NP_001255968.1:n.-29_-16del
NM_007373.3:c.-29_-16del , LRG_753t1:c.-29_-16del	NP_031399.2:n.-29_-16del
XM_011540216.1:c.-380-21298_-380-21285del	XP_011538518.1:n.-380-21298_-380-21285del
NM_001269039.2:c.-29_-16del	NP_001255968.1:n.-29_-16del
NM_001324336.1:c.-29_-16del	NP_001311265.1:n.-29_-16del
NM_001324337.1:c.-29_-16del	NP_001311266.1:n.-29_-16del
NR_136749.1:n.116-21298_116-21285del
NM_007373.4:c.-29_-16del MANE Select	NP_031399.2:n.-29_-16del
NM_001269039.3:c.-29_-16del	NP_001255968.1:n.-29_-16del
NM_001324336.2:c.-29_-16del	NP_001311265.1:n.-29_-16del
NM_001324337.2:c.-29_-16del	NP_001311266.1:n.-29_-16del
NR_136749.2:n.55-21298_55-21285del