Canonical Allele Identifier: CA566689150

Gene: HLA-B

Linked Data

• gnomAD v2: 6-31324539-A-ACTT
• gnomAD v3: 6-31356762-A-ACTT
• gnomAD v4: 6-31356762-A-ACTT
• MyVariant Identifiers: chr6:g.31324539_31324540insCTT (hg19) ; chr6:g.31356762_31356763insCTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356762_31356763insCTT , CM000668.2:g.31356762_31356763insCTT	GRCh38
NC_000006.11:g.31324539_31324540insCTT , CM000668.1:g.31324539_31324540insCTT	GRCh37
NC_000006.10:g.31432518_31432519insCTT	NCBI36
NG_023187.1:g.5450_5451insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1741_1742insAAG
ENST00000481849.6:n.1741_1742insAAG
ENST00000497377.6:n.1741_1742insAAG
ENST00000640094.2:c.268_269insAAG	ENSP00000491275.2:p.Ile90delinsLysVal
ENST00000696558.1:c.268_269insAAG	ENSP00000512716.1:p.Ile90delinsLysVal
ENST00000696559.1:c.268_269insAAG	ENSP00000512717.1:p.Ile90delinsLysVal
ENST00000696560.1:c.268_269insAAG	ENSP00000512718.1:p.Ile90delinsLysVal
ENST00000696561.1:c.268_269insAAG	ENSP00000512719.1:p.Ile90delinsLysVal
ENST00000696562.1:c.268_269insAAG	ENSP00000512720.1:p.Ile90delinsLysVal
ENST00000412585.7:c.268_269insAAG MANE Select	ENSP00000399168.2:p.Ile90delinsLysVal
ENST00000412585.6:c.268_269insAAG	ENSP00000399168.2:p.Ile90delinsLysVal
ENST00000434333.1:c.301_302insAAG	ENSP00000405931.1:p.Ile101delinsLysVal
ENST00000474381.1:n.143_144insAAG
ENST00000498007.1:n.289_290insAAG
ENST00000603274.1:n.116_117insCTT
NM_005514.6:c.268_269insAAG	NP_005505.2:p.Ile90delinsLysVal
XM_011514556.1:c.301_302insAAG	XP_011512858.1:p.Ile101delinsLysVal
XM_011514557.1:c.268_269insAAG	XP_011512859.1:p.Ile90delinsLysVal
XR_926175.1:n.278_279insAAG
NM_005514.7:c.268_269insAAG	NP_005505.2:p.Ile90delinsLysVal
NM_005514.8:c.268_269insAAG MANE Select	NP_005505.2:p.Ile90delinsLysVal