Canonical Allele Identifier: CA2616532785

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058618-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058618C>T , CM000673.2:g.123058618C>T	GRCh38
NC_000011.9:g.122929326C>T , CM000673.1:g.122929326C>T	GRCh37
NC_000011.8:g.122434536C>T	NCBI36
NG_029473.1:g.8519G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+14G>A MANE Select	ENSP00000432083.1:n.1522+14G>A
ENST00000227378.7:c.1522+14G>A	ENSP00000227378.3:n.1522+14G>A
ENST00000453788.6:c.1387+149G>A	ENSP00000404372.2:n.1387+149G>A
ENST00000524552.5:c.295+14G>A	ENSP00000435908.1:n.295+14G>A
ENST00000526110.5:c.1465+14G>A	ENSP00000433584.1:n.1465+14G>A
ENST00000526686.1:c.178+14G>A	ENSP00000435019.1:n.178+14G>A
ENST00000532091.1:n.1511G>A
ENST00000532636.5:c.1522+14G>A	ENSP00000437125.1:n.1522+14G>A
ENST00000533540.5:c.1084+14G>A	ENSP00000437189.1:n.1084+14G>A
ENST00000534319.5:c.814+14G>A	ENSP00000433316.1:n.814+14G>A
ENST00000534624.5:c.1522+14G>A	ENSP00000432083.1:n.1522+14G>A
NM_006597.5:c.1522+14G>A	NP_006588.1:n.1522+14G>A
NM_153201.3:c.1387+149G>A	NP_694881.1:n.1387+149G>A
XM_011542798.1:c.1522+14G>A	XP_011541100.1:n.1522+14G>A
NM_006597.6:c.1522+14G>A MANE Select	NP_006588.1:n.1522+14G>A
NM_153201.4:c.1387+149G>A	NP_694881.1:n.1387+149G>A