Canonical Allele Identifier: CA383057490

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058827-A-G
• COSMIC: COSM1297758
• MyVariant Identifiers: chr11:g.122929535A>G (hg19) ; chr11:g.123058827A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058827A>G , CM000673.2:g.123058827A>G	GRCh38
NC_000011.9:g.122929535A>G , CM000673.1:g.122929535A>G	GRCh37
NC_000011.8:g.122434745A>G	NCBI36
NG_029473.1:g.8310T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000534624.6:c.1327T>C MANE Select	ENSP00000432083.1:p.Tyr443His
ENST00000227378.7:c.1327T>C	ENSP00000227378.3:p.Tyr443His
ENST00000453788.6:c.1327T>C	ENSP00000404372.2:p.Tyr443His
ENST00000524552.5:c.100T>C	ENSP00000435908.1:p.Tyr34His
ENST00000526110.5:c.1270T>C	ENSP00000433584.1:p.Tyr424His
ENST00000526686.1:c.-18T>C	ENSP00000435019.1:n.-18T>C
ENST00000532091.1:n.1302T>C
ENST00000532636.5:c.1327T>C	ENSP00000437125.1:p.Tyr443His
ENST00000533238.5:n.429T>C
ENST00000533540.5:c.889T>C	ENSP00000437189.1:p.Tyr297His
ENST00000534319.5:c.619T>C	ENSP00000433316.1:p.Tyr207His
ENST00000534624.5:c.1327T>C	ENSP00000432083.1:p.Tyr443His
NM_006597.5:c.1327T>C	NP_006588.1:p.Tyr443His
NM_153201.3:c.1327T>C	NP_694881.1:p.Tyr443His
XM_011542798.1:c.1327T>C	XP_011541100.1:p.Tyr443His
NM_006597.6:c.1327T>C MANE Select	NP_006588.1:p.Tyr443His
NM_153201.4:c.1327T>C	NP_694881.1:p.Tyr443His