Canonical Allele Identifier: CA2005597602

Gene: HSPA8 SNORD14C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123059354A= , CM000673.2:g.123059354A=	GRCh38
NC_000011.9:g.122930062A= , CM000673.1:g.122930062A=	GRCh37
NC_000011.8:g.122435272A=	NCBI36
NG_029473.1:g.7783T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1121-93T= (HSPA8) MANE Select	ENSP00000432083.1:n.1121-93T=
ENST00000227378.7:c.1121-93T= (HSPA8)	ENSP00000227378.3:n.1121-93T=
ENST00000453788.6:c.1121-93T= (HSPA8)	ENSP00000404372.2:n.1121-93T=
ENST00000524552.5:c.-200T= (HSPA8)	ENSP00000435908.1:n.-200T=
ENST00000526110.5:c.1064-93T= (HSPA8)	ENSP00000433584.1:n.1064-93T=
ENST00000526862.1:n.399-93T= (HSPA8)
ENST00000527983.5:n.1388T= (HSPA8)
ENST00000532091.1:n.868-93T= (HSPA8)
ENST00000532636.5:c.1121-93T= (HSPA8)	ENSP00000437125.1:n.1121-93T=
ENST00000533238.5:n.381-251T= (HSPA8)
ENST00000533540.5:c.683-93T= (HSPA8)	ENSP00000437189.1:n.683-93T=
ENST00000534319.5:c.413-93T= (HSPA8)	ENSP00000433316.1:n.413-93T=
ENST00000534624.5:c.1121-93T= (HSPA8)	ENSP00000432083.1:n.1121-93T=
NM_006597.5:c.1121-93T= (HSPA8)	NP_006588.1:n.1121-93T=
NM_153201.3:c.1121-93T= (HSPA8)	NP_694881.1:n.1121-93T=
NR_001453.2:n.69T= (SNORD14C)
XM_011542798.1:c.1121-93T= (HSPA8)	XP_011541100.1:n.1121-93T=
NM_006597.6:c.1121-93T= (HSPA8) MANE Select	NP_006588.1:n.1121-93T=
NM_153201.4:c.1121-93T= (HSPA8)	NP_694881.1:n.1121-93T=