Canonical Allele Identifier: CA6332567
Gene: HSPA8 HGNC NCBI

Linked Data

dbSNP Id: rs762934951

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123059308_123059348dup , CM000673.2:g.123059308_123059348dup GRCh38
NC_000011.9:g.122930016_122930056dup , CM000673.1:g.122930016_122930056dup GRCh37
NC_000011.8:g.122435226_122435266dup NCBI36
NG_029473.1:g.7789_7829dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1121-87_1121-47dup MANE Select ENSP00000432083.1:n.1121-87_1121-47dup
ENST00000227378.7:c.1121-87_1121-47dup ENSP00000227378.3:n.1121-87_1121-47dup
ENST00000453788.6:c.1121-87_1121-47dup ENSP00000404372.2:n.1121-87_1121-47dup
ENST00000524552.5:c.-194_-154dup ENSP00000435908.1:n.-194_-154dup
ENST00000526110.5:c.1064-87_1064-47dup ENSP00000433584.1:n.1064-87_1064-47dup
ENST00000526862.1:n.399-87_399-47dup
ENST00000527983.5:n.1394_1434dup
ENST00000532091.1:n.868-87_868-47dup
ENST00000532636.5:c.1121-87_1121-47dup ENSP00000437125.1:n.1121-87_1121-47dup
ENST00000533238.5:n.381-245_381-205dup
ENST00000533540.5:c.683-87_683-47dup ENSP00000437189.1:n.683-87_683-47dup
ENST00000534319.5:c.413-87_413-47dup ENSP00000433316.1:n.413-87_413-47dup
ENST00000534624.5:c.1121-87_1121-47dup ENSP00000432083.1:n.1121-87_1121-47dup
NM_006597.5:c.1121-87_1121-47dup NP_006588.1:n.1121-87_1121-47dup
NM_153201.3:c.1121-87_1121-47dup NP_694881.1:n.1121-87_1121-47dup
XM_011542798.1:c.1121-87_1121-47dup XP_011541100.1:n.1121-87_1121-47dup
NM_006597.6:c.1121-87_1121-47dup MANE Select NP_006588.1:n.1121-87_1121-47dup
NM_153201.4:c.1121-87_1121-47dup NP_694881.1:n.1121-87_1121-47dup