Canonical Allele Identifier: CA6332560

Gene: HSPA8

Linked Data

• dbSNP Id: rs772986398
• ExAC: 11:122930002 T / TA
• gnomAD v2: 11-122930002-T-TA
• gnomAD v3: 11-123059294-T-TA
• gnomAD v4: 11-123059294-T-TA
• MyVariant Identifiers: chr11:g.122930002_122930003insA (hg19) ; chr11:g.123059294_123059295insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059298dup , CM000673.2:g.123059298dup	GRCh38
NC_000011.9:g.122930006dup , CM000673.1:g.122930006dup	GRCh37
NC_000011.8:g.122435216dup	NCBI36
NG_029473.1:g.7842dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-34dup MANE Select	ENSP00000432083.1:n.1121-34dup
ENST00000227378.7:c.1121-34dup	ENSP00000227378.3:n.1121-34dup
ENST00000453788.6:c.1121-34dup	ENSP00000404372.2:n.1121-34dup
ENST00000524552.5:c.-141dup	ENSP00000435908.1:n.-141dup
ENST00000526110.5:c.1064-34dup	ENSP00000433584.1:n.1064-34dup
ENST00000526862.1:n.399-34dup
ENST00000527983.5:n.1447dup
ENST00000532091.1:n.868-34dup
ENST00000532636.5:c.1121-34dup	ENSP00000437125.1:n.1121-34dup
ENST00000533238.5:n.381-192dup
ENST00000533540.5:c.683-34dup	ENSP00000437189.1:n.683-34dup
ENST00000534319.5:c.413-34dup	ENSP00000433316.1:n.413-34dup
ENST00000534624.5:c.1121-34dup	ENSP00000432083.1:n.1121-34dup
NM_006597.5:c.1121-34dup	NP_006588.1:n.1121-34dup
NM_153201.3:c.1121-34dup	NP_694881.1:n.1121-34dup
XM_011542798.1:c.1121-34dup	XP_011541100.1:n.1121-34dup
NM_006597.6:c.1121-34dup MANE Select	NP_006588.1:n.1121-34dup
NM_153201.4:c.1121-34dup	NP_694881.1:n.1121-34dup