Canonical Allele Identifier: CA6332563

Gene: HSPA8

Linked Data

• dbSNP Id: rs746913030
• ExAC: 11:122930007 G / A
• gnomAD v2: 11-122930007-G-A
• gnomAD v3: 11-123059299-G-A
• gnomAD v4: 11-123059299-G-A
• MyVariant Identifiers: chr11:g.122930007G>A (hg19) ; chr11:g.122930007_122930008delinsAA (hg19) ; chr11:g.123059299G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059299G>A , CM000673.2:g.123059299G>A	GRCh38
NC_000011.9:g.122930007G>A , CM000673.1:g.122930007G>A	GRCh37
NC_000011.8:g.122435217G>A	NCBI36
NG_029473.1:g.7838C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-38C>T MANE Select	ENSP00000432083.1:n.1121-38C>T
ENST00000227378.7:c.1121-38C>T	ENSP00000227378.3:n.1121-38C>T
ENST00000453788.6:c.1121-38C>T	ENSP00000404372.2:n.1121-38C>T
ENST00000524552.5:c.-145C>T	ENSP00000435908.1:n.-145C>T
ENST00000526110.5:c.1064-38C>T	ENSP00000433584.1:n.1064-38C>T
ENST00000526862.1:n.399-38C>T
ENST00000527983.5:n.1443C>T
ENST00000532091.1:n.868-38C>T
ENST00000532636.5:c.1121-38C>T	ENSP00000437125.1:n.1121-38C>T
ENST00000533238.5:n.381-196C>T
ENST00000533540.5:c.683-38C>T	ENSP00000437189.1:n.683-38C>T
ENST00000534319.5:c.413-38C>T	ENSP00000433316.1:n.413-38C>T
ENST00000534624.5:c.1121-38C>T	ENSP00000432083.1:n.1121-38C>T
NM_006597.5:c.1121-38C>T	NP_006588.1:n.1121-38C>T
NM_153201.3:c.1121-38C>T	NP_694881.1:n.1121-38C>T
XM_011542798.1:c.1121-38C>T	XP_011541100.1:n.1121-38C>T
NM_006597.6:c.1121-38C>T MANE Select	NP_006588.1:n.1121-38C>T
NM_153201.4:c.1121-38C>T	NP_694881.1:n.1121-38C>T