Canonical Allele Identifier: CA2616532720
Gene: HSPA8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.123058464_123058465insATGCTTT , CM000673.2:g.123058464_123058465insATGCTTT GRCh38
NC_000011.9:g.122929172_122929173insATGCTTT , CM000673.1:g.122929172_122929173insATGCTTT GRCh37
NC_000011.8:g.122434382_122434383insATGCTTT NCBI36
NG_029473.1:g.8673_8674insAAGCATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000534624.6:c.1543_1544insAAGCATA MANE Select ENSP00000432083.1:p.Ile515LysfsTer4
ENST00000227378.7:c.1543_1544insAAGCATA ENSP00000227378.3:p.Ile515LysfsTer4
ENST00000453788.6:c.1387+303_1387+304insAAGCATA ENSP00000404372.2:n.1387+303_1387+304insAAGCATA
ENST00000524552.5:c.316_317insAAGCATA ENSP00000435908.1:p.Ile106LysfsTer4
ENST00000526110.5:c.1486_1487insAAGCATA ENSP00000433584.1:p.Ile496LysfsTer4
ENST00000526686.1:c.199_200insAAGCATA ENSP00000435019.1:p.Ile67LysfsTer4
ENST00000532091.1:n.1665_1666insAAGCATA
ENST00000532636.5:c.1543_1544insAAGCATA ENSP00000437125.1:p.Ile515LysfsTer4
ENST00000533540.5:c.1105_1106insAAGCATA ENSP00000437189.1:p.Ile369LysfsTer4
ENST00000534319.5:c.835_836insAAGCATA ENSP00000433316.1:p.Ile279LysfsTer4
ENST00000534624.5:c.1543_1544insAAGCATA ENSP00000432083.1:p.Ile515LysfsTer4
NM_006597.5:c.1543_1544insAAGCATA NP_006588.1:p.Ile515LysfsTer4
NM_153201.3:c.1387+303_1387+304insAAGCATA NP_694881.1:n.1387+303_1387+304insAAGCATA
XM_011542798.1:c.1543_1544insAAGCATA XP_011541100.1:p.Ile515LysfsTer4
NM_006597.6:c.1543_1544insAAGCATA MANE Select NP_006588.1:p.Ile515LysfsTer4
NM_153201.4:c.1387+303_1387+304insAAGCATA NP_694881.1:n.1387+303_1387+304insAAGCATA