Canonical Allele Identifier: CA566285816

Gene: HLA-A

Linked Data

• dbSNP Id: rs1182601677
• gnomAD v2: 6-29911066-TGTA-T
• gnomAD v4: 6-29943289-TGTA-T
• MyVariant Identifiers: chr6:g.29911067_29911069del (hg19) ; chr6:g.29943290_29943292del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29943290_29943292del , CM000668.2:g.29943290_29943292del	GRCh38
NC_000006.11:g.29911067_29911069del , CM000668.1:g.29911067_29911069del	GRCh37
NC_000006.10:g.30019046_30019048del	NCBI36
NG_029217.2:g.5825_5827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638375.2:c.366_368del	ENSP00000492789.2:p.Met122_Tyr123delinsIle
ENST00000706892.1:n.642_644del
ENST00000706893.1:c.366_368del	ENSP00000516609.1:p.Met122_Tyr123delinsIle
ENST00000706894.1:c.366_368del	ENSP00000516610.1:p.Met122_Tyr123delinsIle
ENST00000706895.1:n.642_644del
ENST00000706896.1:n.642_644del
ENST00000706897.1:n.642_644del
ENST00000706898.1:c.366_368del	ENSP00000516611.1:p.Met122_Tyr123delinsIle
ENST00000706899.1:n.642_644del
ENST00000706900.1:c.282_284del	ENSP00000516617.1:p.Met94_Tyr95delinsIle
ENST00000706901.1:c.366_368del	ENSP00000516612.1:p.Met122_Tyr123delinsIle
ENST00000706902.1:c.366_368del	ENSP00000516613.1:p.Met122_Tyr123delinsIle
ENST00000706903.1:c.366_368del	ENSP00000516614.1:p.Met122_Tyr123delinsIle
ENST00000706904.1:c.366_368del	ENSP00000516615.1:p.Met122_Tyr123delinsIle
ENST00000706905.1:c.366_368del	ENSP00000516616.1:p.Met122_Tyr123delinsIle
ENST00000376809.10:c.366_368del MANE Select	ENSP00000366005.5:p.Met122_Tyr123delinsIle
ENST00000638375.1:c.366_368del	ENSP00000492789.1:p.Met122_Tyr123delinsIle
ENST00000376802.2:c.366_368del	ENSP00000365998.2:p.Met122_Tyr123delinsIle
ENST00000376806.9:c.366_368del	ENSP00000366002.5:p.Met122_Tyr123delinsIle
ENST00000376809.9:c.366_368del	ENSP00000366005.5:p.Met122_Tyr123delinsIle
ENST00000396634.5:c.366_368del	ENSP00000379873.1:p.Met122_Tyr123delinsIle
ENST00000461903.1:n.607_609del
ENST00000479320.5:n.607_609del
ENST00000495183.5:n.609_611del
ENST00000496081.5:n.183_185del
NM_002116.7:c.366_368del	NP_002107.3:p.Met122_Tyr123delinsIle
NM_002116.8:c.366_368del MANE Select	NP_002107.3:p.Met122_Tyr123delinsIle