Canonical Allele Identifier: CA383058528

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123059222-T-C
• MyVariant Identifiers: chr11:g.122929930T>C (hg19) ; chr11:g.123059222T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059222T>C , CM000673.2:g.123059222T>C	GRCh38
NC_000011.9:g.122929930T>C , CM000673.1:g.122929930T>C	GRCh37
NC_000011.8:g.122435140T>C	NCBI36
NG_029473.1:g.7915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1160A>G MANE Select	ENSP00000432083.1:p.Asn387Ser
ENST00000227378.7:c.1160A>G	ENSP00000227378.3:p.Asn387Ser
ENST00000453788.6:c.1160A>G	ENSP00000404372.2:p.Asn387Ser
ENST00000524552.5:c.-68A>G	ENSP00000435908.1:n.-68A>G
ENST00000526110.5:c.1103A>G	ENSP00000433584.1:p.Asn368Ser
ENST00000526862.1:n.438A>G
ENST00000532091.1:n.907A>G
ENST00000532636.5:c.1160A>G	ENSP00000437125.1:p.Asn387Ser
ENST00000533238.5:n.381-119A>G
ENST00000533540.5:c.722A>G	ENSP00000437189.1:p.Asn241Ser
ENST00000534319.5:c.452A>G	ENSP00000433316.1:p.Asn151Ser
ENST00000534624.5:c.1160A>G	ENSP00000432083.1:p.Asn387Ser
NM_006597.5:c.1160A>G	NP_006588.1:p.Asn387Ser
NM_153201.3:c.1160A>G	NP_694881.1:p.Asn387Ser
XM_011542798.1:c.1160A>G	XP_011541100.1:p.Asn387Ser
NM_006597.6:c.1160A>G MANE Select	NP_006588.1:p.Asn387Ser
NM_153201.4:c.1160A>G	NP_694881.1:p.Asn387Ser