Canonical Allele Identifier: CA602581068

Gene: HSPA8

Linked Data

• dbSNP Id: rs575956745
• gnomAD v2: 11-122929237-G-GTT
• gnomAD v3: 11-123058529-G-GTT
• gnomAD v4: 11-123058529-G-GTT
• MyVariant Identifiers: chr11:g.122929237_122929238insTT (hg19) ; chr11:g.123058529_123058530insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058530_123058531insTT , CM000673.2:g.123058530_123058531insTT	GRCh38
NC_000011.9:g.122929238_122929239insTT , CM000673.1:g.122929238_122929239insTT	GRCh37
NC_000011.8:g.122434448_122434449insTT	NCBI36
NG_029473.1:g.8607_8608insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1523-46_1523-45insAA MANE Select	ENSP00000432083.1:n.1523-46_1523-45insAA
ENST00000227378.7:c.1523-46_1523-45insAA	ENSP00000227378.3:n.1523-46_1523-45insAA
ENST00000453788.6:c.1387+237_1387+238insAA	ENSP00000404372.2:n.1387+237_1387+238insAA
ENST00000524552.5:c.296-46_296-45insAA	ENSP00000435908.1:n.296-46_296-45insAA
ENST00000526110.5:c.1466-46_1466-45insAA	ENSP00000433584.1:n.1466-46_1466-45insAA
ENST00000526686.1:c.179-46_179-45insAA	ENSP00000435019.1:n.179-46_179-45insAA
ENST00000532091.1:n.1599_1600insAA
ENST00000532636.5:c.1523-46_1523-45insAA	ENSP00000437125.1:n.1523-46_1523-45insAA
ENST00000533540.5:c.1085-46_1085-45insAA	ENSP00000437189.1:n.1085-46_1085-45insAA
ENST00000534319.5:c.815-46_815-45insAA	ENSP00000433316.1:n.815-46_815-45insAA
ENST00000534624.5:c.1523-46_1523-45insAA	ENSP00000432083.1:n.1523-46_1523-45insAA
NM_006597.5:c.1523-46_1523-45insAA	NP_006588.1:n.1523-46_1523-45insAA
NM_153201.3:c.1387+237_1387+238insAA	NP_694881.1:n.1387+237_1387+238insAA
XM_011542798.1:c.1523-46_1523-45insAA	XP_011541100.1:n.1523-46_1523-45insAA
NM_006597.6:c.1523-46_1523-45insAA MANE Select	NP_006588.1:n.1523-46_1523-45insAA
NM_153201.4:c.1387+237_1387+238insAA	NP_694881.1:n.1387+237_1387+238insAA