Canonical Allele Identifier: CA2005594933
Gene: HSPA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058517_123058518delinsTA , CM000673.2:g.123058517_123058518delinsTA GRCh38
NC_000011.9:g.122929225_122929226delinsTA , CM000673.1:g.122929225_122929226delinsTA GRCh37
NC_000011.8:g.122434435_122434436delinsTA NCBI36
NG_029473.1:g.8619_8620delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1523-34_1523-33delinsTA MANE Select ENSP00000432083.1:n.1523-34_1523-33delinsTA
ENST00000227378.7:c.1523-34_1523-33delinsTA ENSP00000227378.3:n.1523-34_1523-33delinsTA
ENST00000453788.6:c.1387+249_1387+250delinsTA ENSP00000404372.2:n.1387+249_1387+250delinsTA
ENST00000524552.5:c.296-34_296-33delinsTA ENSP00000435908.1:n.296-34_296-33delinsTA
ENST00000526110.5:c.1466-34_1466-33delinsTA ENSP00000433584.1:n.1466-34_1466-33delinsTA
ENST00000526686.1:c.179-34_179-33delinsTA ENSP00000435019.1:n.179-34_179-33delinsTA
ENST00000532091.1:n.1611_1612delinsTA
ENST00000532636.5:c.1523-34_1523-33delinsTA ENSP00000437125.1:n.1523-34_1523-33delinsTA
ENST00000533540.5:c.1085-34_1085-33delinsTA ENSP00000437189.1:n.1085-34_1085-33delinsTA
ENST00000534319.5:c.815-34_815-33delinsTA ENSP00000433316.1:n.815-34_815-33delinsTA
ENST00000534624.5:c.1523-34_1523-33delinsTA ENSP00000432083.1:n.1523-34_1523-33delinsTA
NM_006597.5:c.1523-34_1523-33delinsTA NP_006588.1:n.1523-34_1523-33delinsTA
NM_153201.3:c.1387+249_1387+250delinsTA NP_694881.1:n.1387+249_1387+250delinsTA
XM_011542798.1:c.1523-34_1523-33delinsTA XP_011541100.1:n.1523-34_1523-33delinsTA
NM_006597.6:c.1523-34_1523-33delinsTA MANE Select NP_006588.1:n.1523-34_1523-33delinsTA
NM_153201.4:c.1387+249_1387+250delinsTA NP_694881.1:n.1387+249_1387+250delinsTA