Canonical Allele Identifier: CA229966779

Gene: HSPA8

Linked Data

• dbSNP Id: rs34958717
• MyVariant Identifiers: chr11:g.122929338_122929339insC (hg19) ; chr11:g.123058630_123058631insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058633dup , CM000673.2:g.123058633dup	GRCh38
NC_000011.9:g.122929341dup , CM000673.1:g.122929341dup	GRCh37
NC_000011.8:g.122434551dup	NCBI36
NG_029473.1:g.8506dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+1dup
ENST00000227378.7:c.1522+1dup
ENST00000453788.6:c.1387+136dup	ENSP00000404372.2:n.1387+136dup
ENST00000524552.5:c.295+1dup
ENST00000526110.5:c.1465+1dup
ENST00000526686.1:c.178+1dup
ENST00000532091.1:n.1498dup
ENST00000532636.5:c.1522+1dup
ENST00000533540.5:c.1084+1dup
ENST00000534319.5:c.814+1dup
ENST00000534624.5:c.1522+1dup
NM_006597.5:c.1522+1dup
NM_153201.3:c.1387+136dup	NP_694881.1:n.1387+136dup
XM_011542798.1:c.1522+1dup
NM_006597.6:c.1522+1dup
NM_153201.4:c.1387+136dup	NP_694881.1:n.1387+136dup