Canonical Allele Identifier: CA2388907389

Gene: ERG

Linked Data

• dbSNP Id: rs1989218420
• gnomAD v3: 21-38415061-AAC-A
• gnomAD v4: 21-38415061-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38415065_38415066del , CM000683.2:g.38415065_38415066del	GRCh38
NC_000021.8:g.39786987_39786988del , CM000683.1:g.39786987_39786988del	GRCh37
NC_000021.7:g.38708857_38708858del	NCBI36
NG_029732.1:g.251720_251721del

Transcript Alleles

HGVS	Amino-acid change
ENST00000288319.12:c.388+8347_388+8348del MANE Select	ENSP00000288319.7:n.388+8347_388+8348del
ENST00000288319.11:c.388+8347_388+8348del	ENSP00000288319.7:n.388+8347_388+8348del
ENST00000398897.5:c.112+8347_112+8348del	ENSP00000381871.1:n.112+8347_112+8348del
ENST00000398905.5:c.388+8347_388+8348del	ENSP00000381877.1:n.388+8347_388+8348del
ENST00000398907.5:c.388+8347_388+8348del	ENSP00000381879.1:n.388+8347_388+8348del
ENST00000398910.5:c.409+8347_409+8348del	ENSP00000381881.1:n.409+8347_409+8348del
ENST00000398911.5:c.409+8347_409+8348del	ENSP00000381882.1:n.409+8347_409+8348del
ENST00000398919.6:c.409+8347_409+8348del	ENSP00000381891.2:n.409+8347_409+8348del
ENST00000417133.6:c.409+8347_409+8348del	ENSP00000414150.2:n.409+8347_409+8348del
ENST00000429727.6:c.292+8347_292+8348del	ENSP00000415659.3:n.292+8347_292+8348del
ENST00000442448.5:c.409+8347_409+8348del	ENSP00000394694.1:n.409+8347_409+8348del
ENST00000453032.6:c.112+8347_112+8348del	ENSP00000396268.2:n.112+8347_112+8348del
ENST00000468474.5:n.595+8347_595+8348del
ENST00000473107.1:n.454+8347_454+8348del
ENST00000481609.5:n.559+8347_559+8348del
ENST00000492833.5:n.370+8347_370+8348del
NM_001136154.1:c.409+8347_409+8348del	NP_001129626.1:n.409+8347_409+8348del
NM_001136155.1:c.112+8347_112+8348del	NP_001129627.1:n.112+8347_112+8348del
NM_001243428.1:c.409+8347_409+8348del	NP_001230357.1:n.409+8347_409+8348del
NM_001243429.1:c.112+8347_112+8348del	NP_001230358.1:n.112+8347_112+8348del
NM_001243432.2:c.409+8347_409+8348del	NP_001230361.1:n.409+8347_409+8348del
NM_001291391.1:c.409+8347_409+8348del	NP_001278320.1:n.409+8347_409+8348del
NM_004449.4:c.409+8347_409+8348del	NP_004440.1:n.409+8347_409+8348del
NM_182918.3:c.388+8347_388+8348del	NP_891548.1:n.388+8347_388+8348del
XM_011529486.1:c.409+8347_409+8348del	XP_011527788.1:n.409+8347_409+8348del
XM_011529487.1:c.409+8347_409+8348del	XP_011527789.1:n.409+8347_409+8348del
NM_001331025.1:c.388+8347_388+8348del	NP_001317954.1:n.388+8347_388+8348del
NM_182918.4:c.388+8347_388+8348del MANE Select	NP_891548.1:n.388+8347_388+8348del
NM_001331025.2:c.388+8347_388+8348del	NP_001317954.1:n.388+8347_388+8348del