Canonical Allele Identifier: CA2677793818

Gene: HLA-A

Linked Data

• gnomAD v4: 6-29942681-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29942682_29942683del , CM000668.2:g.29942682_29942683del	GRCh38
NC_000006.11:g.29910459_29910460del , CM000668.1:g.29910459_29910460del	GRCh37
NC_000006.10:g.30018438_30018439del	NCBI36
NG_029217.2:g.5217_5218del

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.73+56_73+57del	ENSP00000492789.2:n.73+56_73+57del
ENST00000706892.1:n.349+56_349+57del
ENST00000706893.1:c.73+56_73+57del	ENSP00000516609.1:n.73+56_73+57del
ENST00000706894.1:c.73+56_73+57del	ENSP00000516610.1:n.73+56_73+57del
ENST00000706895.1:n.349+56_349+57del
ENST00000706896.1:n.349+56_349+57del
ENST00000706897.1:n.349+56_349+57del
ENST00000706898.1:c.73+56_73+57del	ENSP00000516611.1:n.73+56_73+57del
ENST00000706899.1:n.349+56_349+57del
ENST00000706901.1:c.73+56_73+57del	ENSP00000516612.1:n.73+56_73+57del
ENST00000706902.1:c.73+56_73+57del	ENSP00000516613.1:n.73+56_73+57del
ENST00000706903.1:c.73+56_73+57del	ENSP00000516614.1:n.73+56_73+57del
ENST00000706904.1:c.73+56_73+57del	ENSP00000516615.1:n.73+56_73+57del
ENST00000706905.1:c.73+56_73+57del	ENSP00000516616.1:n.73+56_73+57del
ENST00000376809.10:c.73+56_73+57del MANE Select	ENSP00000366005.5:n.73+56_73+57del
ENST00000638375.1:c.73+56_73+57del	ENSP00000492789.1:n.73+56_73+57del
ENST00000376802.2:c.73+56_73+57del	ENSP00000365998.2:n.73+56_73+57del
ENST00000376806.9:c.73+56_73+57del	ENSP00000366002.5:n.73+56_73+57del
ENST00000376809.9:c.73+56_73+57del	ENSP00000366005.5:n.73+56_73+57del
ENST00000396634.5:c.73+56_73+57del	ENSP00000379873.1:n.73+56_73+57del
ENST00000429656.1:n.385_386del
ENST00000461903.1:n.73+56_73+57del
ENST00000479320.5:n.73+56_73+57del
ENST00000495183.5:n.75+56_75+57del
ENST00000496081.5:n.79+56_79+57del
NM_002116.7:c.73+56_73+57del	NP_002107.3:n.73+56_73+57del
NM_002116.8:c.73+56_73+57del MANE Select	NP_002107.3:n.73+56_73+57del