Canonical Allele Identifier: CA2005597076

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059212_123059222delinsATCTTGAACAT , CM000673.2:g.123059212_123059222delinsATCTTGAACAT	GRCh38
NC_000011.9:g.122929920_122929930delinsATCTTGAACAT , CM000673.1:g.122929920_122929930delinsATCTTGAACAT	GRCh37
NC_000011.8:g.122435130_122435140delinsATCTTGAACAT	NCBI36
NG_029473.1:g.7915_7925delinsATGTTCAAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1160_1170delinsATGTTCAAGAT MANE Select	ENSP00000432083.1:p.Asn387=
ENST00000227378.7:c.1160_1170delinsATGTTCAAGAT	ENSP00000227378.3:p.Asn387=
ENST00000453788.6:c.1160_1170delinsATGTTCAAGAT	ENSP00000404372.2:p.Asn387=
ENST00000524552.5:c.-68_-58delinsATGTTCAAGAT	ENSP00000435908.1:n.-68_-58delinsATGTTCAAGAT
ENST00000526110.5:c.1103_1113delinsATGTTCAAGAT	ENSP00000433584.1:p.Asn368=
ENST00000526862.1:n.438_448delinsATGTTCAAGAT
ENST00000532091.1:n.907_917delinsATGTTCAAGAT
ENST00000532636.5:c.1160_1170delinsATGTTCAAGAT	ENSP00000437125.1:p.Asn387=
ENST00000533238.5:n.381-119_381-109delinsATGTTCAAGAT
ENST00000533540.5:c.722_732delinsATGTTCAAGAT	ENSP00000437189.1:p.Asn241=
ENST00000534319.5:c.452_462delinsATGTTCAAGAT	ENSP00000433316.1:p.Asn151=
ENST00000534624.5:c.1160_1170delinsATGTTCAAGAT	ENSP00000432083.1:p.Asn387=
NM_006597.5:c.1160_1170delinsATGTTCAAGAT	NP_006588.1:p.Asn387=
NM_153201.3:c.1160_1170delinsATGTTCAAGAT	NP_694881.1:p.Asn387=
XM_011542798.1:c.1160_1170delinsATGTTCAAGAT	XP_011541100.1:p.Asn387=
NM_006597.6:c.1160_1170delinsATGTTCAAGAT MANE Select	NP_006588.1:p.Asn387=
NM_153201.4:c.1160_1170delinsATGTTCAAGAT	NP_694881.1:p.Asn387=