Canonical Allele Identifier: CA3693715

Gene: HLA-A

Linked Data

• dbSNP Id: rs41561414
• ExAC: 6:29912901 T / C
• gnomAD v2: 6-29912901-T-C
• gnomAD v3: 6-29945124-T-C
• gnomAD v4: 6-29945124-T-C
• MyVariant Identifiers: chr6:g.29912901T>C (hg19) ; chr6:g.29945124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.29945124T>C , CM000668.2:g.29945124T>C	GRCh38
NC_000006.11:g.29912901T>C , CM000668.1:g.29912901T>C	GRCh37
NC_000006.10:g.30020880T>C	NCBI36
NG_029217.2:g.7660T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000638375.2:c.928+33T>C	ENSP00000492789.2:n.928+33T>C
ENST00000706892.1:n.2476T>C
ENST00000706893.1:c.*29+33T>C	ENSP00000516609.1:n.*29+33T>C
ENST00000706894.1:c.1045+33T>C	ENSP00000516610.1:n.1045+33T>C
ENST00000706895.1:n.1865+33T>C
ENST00000706896.1:n.2341+33T>C
ENST00000706897.1:n.1763+33T>C
ENST00000706898.1:c.1063+33T>C	ENSP00000516611.1:n.1063+33T>C
ENST00000706899.1:n.1899+33T>C
ENST00000706900.1:c.961+33T>C	ENSP00000516617.1:n.961+33T>C
ENST00000706901.1:c.1045+33T>C	ENSP00000516612.1:n.1045+33T>C
ENST00000706902.1:c.1045+33T>C	ENSP00000516613.1:n.1045+33T>C
ENST00000706903.1:c.1045+33T>C	ENSP00000516614.1:n.1045+33T>C
ENST00000706904.1:c.1045+33T>C	ENSP00000516615.1:n.1045+33T>C
ENST00000706905.1:c.1045+33T>C	ENSP00000516616.1:n.1045+33T>C
ENST00000376809.10:c.1045+33T>C MANE Select	ENSP00000366005.5:n.1045+33T>C
ENST00000638375.1:c.928+33T>C	ENSP00000492789.1:n.928+33T>C
ENST00000376802.2:c.896-327T>C	ENSP00000365998.2:n.896-327T>C
ENST00000376806.9:c.1063+33T>C	ENSP00000366002.5:n.1063+33T>C
ENST00000376809.9:c.1045+33T>C	ENSP00000366005.5:n.1045+33T>C
ENST00000396634.5:c.1045+33T>C	ENSP00000379873.1:n.1045+33T>C
ENST00000461903.1:n.1304+33T>C
ENST00000479320.5:n.1286+33T>C
ENST00000495183.5:n.1284+33T>C
ENST00000496081.5:n.1304+33T>C
NM_002116.7:c.1045+33T>C	NP_002107.3:n.1045+33T>C
NM_002116.8:c.1045+33T>C MANE Select	NP_002107.3:n.1045+33T>C