Canonical Allele Identifier: CA2005597310

Gene: HSPA8

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059281_123059291delinsCGTTAAAAGAA , CM000673.2:g.123059281_123059291delinsCGTTAAAAGAA	GRCh38
NC_000011.9:g.122929989_122929999delinsCGTTAAAAGAA , CM000673.1:g.122929989_122929999delinsCGTTAAAAGAA	GRCh37
NC_000011.8:g.122435199_122435209delinsCGTTAAAAGAA	NCBI36
NG_029473.1:g.7846_7856delinsTTCTTTTAACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-30_1121-20delinsTTCTTTTAACG MANE Select	ENSP00000432083.1:n.1121-30_1121-20delinsTTCTTTTAACG
ENST00000227378.7:c.1121-30_1121-20delinsTTCTTTTAACG	ENSP00000227378.3:n.1121-30_1121-20delinsTTCTTTTAACG
ENST00000453788.6:c.1121-30_1121-20delinsTTCTTTTAACG	ENSP00000404372.2:n.1121-30_1121-20delinsTTCTTTTAACG
ENST00000524552.5:c.-137_-127delinsTTCTTTTAACG	ENSP00000435908.1:n.-137_-127delinsTTCTTTTAACG
ENST00000526110.5:c.1064-30_1064-20delinsTTCTTTTAACG	ENSP00000433584.1:n.1064-30_1064-20delinsTTCTTTTAACG
ENST00000526862.1:n.399-30_399-20delinsTTCTTTTAACG
ENST00000527983.5:n.1451_1461delinsTTCTTTTAACG
ENST00000532091.1:n.868-30_868-20delinsTTCTTTTAACG
ENST00000532636.5:c.1121-30_1121-20delinsTTCTTTTAACG	ENSP00000437125.1:n.1121-30_1121-20delinsTTCTTTTAACG
ENST00000533238.5:n.381-188_381-178delinsTTCTTTTAACG
ENST00000533540.5:c.683-30_683-20delinsTTCTTTTAACG	ENSP00000437189.1:n.683-30_683-20delinsTTCTTTTAACG
ENST00000534319.5:c.413-30_413-20delinsTTCTTTTAACG	ENSP00000433316.1:n.413-30_413-20delinsTTCTTTTAACG
ENST00000534624.5:c.1121-30_1121-20delinsTTCTTTTAACG	ENSP00000432083.1:n.1121-30_1121-20delinsTTCTTTTAACG
NM_006597.5:c.1121-30_1121-20delinsTTCTTTTAACG	NP_006588.1:n.1121-30_1121-20delinsTTCTTTTAACG
NM_153201.3:c.1121-30_1121-20delinsTTCTTTTAACG	NP_694881.1:n.1121-30_1121-20delinsTTCTTTTAACG
XM_011542798.1:c.1121-30_1121-20delinsTTCTTTTAACG	XP_011541100.1:n.1121-30_1121-20delinsTTCTTTTAACG
NM_006597.6:c.1121-30_1121-20delinsTTCTTTTAACG MANE Select	NP_006588.1:n.1121-30_1121-20delinsTTCTTTTAACG
NM_153201.4:c.1121-30_1121-20delinsTTCTTTTAACG	NP_694881.1:n.1121-30_1121-20delinsTTCTTTTAACG