Canonical Allele Identifier: CA383056975

Gene: HSPA8

Linked Data

• dbSNP Id: rs1555074221
• MyVariant Identifiers: chr11:g.122929295_122929296insG (hg19) ; chr11:g.123058587_123058588insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058587_123058588insG , CM000673.2:g.123058587_123058588insG	GRCh38
NC_000011.9:g.122929295_122929296insG , CM000673.1:g.122929295_122929296insG	GRCh37
NC_000011.8:g.122434505_122434506insG	NCBI36
NG_029473.1:g.8549_8550insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+44_1522+45insC MANE Select	ENSP00000432083.1:n.1522+44_1522+45insC
ENST00000227378.7:c.1522+44_1522+45insC	ENSP00000227378.3:n.1522+44_1522+45insC
ENST00000453788.6:c.1387+179_1387+180insC	ENSP00000404372.2:n.1387+179_1387+180insC
ENST00000524552.5:c.295+44_295+45insC	ENSP00000435908.1:n.295+44_295+45insC
ENST00000526110.5:c.1465+44_1465+45insC	ENSP00000433584.1:n.1465+44_1465+45insC
ENST00000526686.1:c.178+44_178+45insC	ENSP00000435019.1:n.178+44_178+45insC
ENST00000532091.1:n.1541_1542insC
ENST00000532636.5:c.1522+44_1522+45insC	ENSP00000437125.1:n.1522+44_1522+45insC
ENST00000533540.5:c.1084+44_1084+45insC	ENSP00000437189.1:n.1084+44_1084+45insC
ENST00000534319.5:c.814+44_814+45insC	ENSP00000433316.1:n.814+44_814+45insC
ENST00000534624.5:c.1522+44_1522+45insC	ENSP00000432083.1:n.1522+44_1522+45insC
NM_006597.5:c.1522+44_1522+45insC	NP_006588.1:n.1522+44_1522+45insC
NM_153201.3:c.1387+179_1387+180insC	NP_694881.1:n.1387+179_1387+180insC
XM_011542798.1:c.1522+44_1522+45insC	XP_011541100.1:n.1522+44_1522+45insC
NM_006597.6:c.1522+44_1522+45insC MANE Select	NP_006588.1:n.1522+44_1522+45insC
NM_153201.4:c.1387+179_1387+180insC	NP_694881.1:n.1387+179_1387+180insC