Canonical Allele Identifier: CA2616532738
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058534_123058535insAATTAACTA , CM000673.2:g.123058534_123058535insAATTAACTA GRCh38
NC_000011.9:g.122929242_122929243insAATTAACTA , CM000673.1:g.122929242_122929243insAATTAACTA GRCh37
NC_000011.8:g.122434452_122434453insAATTAACTA NCBI36
NG_029473.1:g.8602_8603insTAGTTAATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1523-51_1523-50insTAGTTAATT MANE Select ENSP00000432083.1:n.1523-51_1523-50insTAGTTAATT
ENST00000227378.7:c.1523-51_1523-50insTAGTTAATT ENSP00000227378.3:n.1523-51_1523-50insTAGTTAATT
ENST00000453788.6:c.1387+232_1387+233insTAGTTAATT ENSP00000404372.2:n.1387+232_1387+233insTAGTTAATT
ENST00000524552.5:c.296-51_296-50insTAGTTAATT ENSP00000435908.1:n.296-51_296-50insTAGTTAATT
ENST00000526110.5:c.1466-51_1466-50insTAGTTAATT ENSP00000433584.1:n.1466-51_1466-50insTAGTTAATT
ENST00000526686.1:c.179-51_179-50insTAGTTAATT ENSP00000435019.1:n.179-51_179-50insTAGTTAATT
ENST00000532091.1:n.1594_1595insTAGTTAATT
ENST00000532636.5:c.1523-51_1523-50insTAGTTAATT ENSP00000437125.1:n.1523-51_1523-50insTAGTTAATT
ENST00000533540.5:c.1085-51_1085-50insTAGTTAATT ENSP00000437189.1:n.1085-51_1085-50insTAGTTAATT
ENST00000534319.5:c.815-51_815-50insTAGTTAATT ENSP00000433316.1:n.815-51_815-50insTAGTTAATT
ENST00000534624.5:c.1523-51_1523-50insTAGTTAATT ENSP00000432083.1:n.1523-51_1523-50insTAGTTAATT
NM_006597.5:c.1523-51_1523-50insTAGTTAATT NP_006588.1:n.1523-51_1523-50insTAGTTAATT
NM_153201.3:c.1387+232_1387+233insTAGTTAATT NP_694881.1:n.1387+232_1387+233insTAGTTAATT
XM_011542798.1:c.1523-51_1523-50insTAGTTAATT XP_011541100.1:n.1523-51_1523-50insTAGTTAATT
NM_006597.6:c.1523-51_1523-50insTAGTTAATT MANE Select NP_006588.1:n.1523-51_1523-50insTAGTTAATT
NM_153201.4:c.1387+232_1387+233insTAGTTAATT NP_694881.1:n.1387+232_1387+233insTAGTTAATT