Canonical Allele Identifier: CA2616532759

Gene: HSPA8

Linked Data

• gnomAD v4: 11-123058557-A-AGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.123058559_123058561dup , CM000673.2:g.123058559_123058561dup	GRCh38
NC_000011.9:g.122929267_122929269dup , CM000673.1:g.122929267_122929269dup	GRCh37
NC_000011.8:g.122434477_122434479dup	NCBI36
NG_029473.1:g.8577_8579dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534624.6:c.1522+72_1523-74dup MANE Select	ENSP00000432083.1:n.1522+72_1523-74dup
ENST00000227378.7:c.1522+72_1523-74dup	ENSP00000227378.3:n.1522+72_1523-74dup
ENST00000453788.6:c.1387+207_1387+209dup	ENSP00000404372.2:n.1387+207_1387+209dup
ENST00000524552.5:c.295+72_296-74dup	ENSP00000435908.1:n.295+72_296-74dup
ENST00000526110.5:c.1465+72_1466-74dup	ENSP00000433584.1:n.1465+72_1466-74dup
ENST00000526686.1:c.178+72_179-74dup	ENSP00000435019.1:n.178+72_179-74dup
ENST00000532091.1:n.1569_1571dup
ENST00000532636.5:c.1522+72_1523-74dup	ENSP00000437125.1:n.1522+72_1523-74dup
ENST00000533540.5:c.1084+72_1085-74dup	ENSP00000437189.1:n.1084+72_1085-74dup
ENST00000534319.5:c.814+72_815-74dup	ENSP00000433316.1:n.814+72_815-74dup
ENST00000534624.5:c.1522+72_1523-74dup	ENSP00000432083.1:n.1522+72_1523-74dup
NM_006597.5:c.1522+72_1523-74dup	NP_006588.1:n.1522+72_1523-74dup
NM_153201.3:c.1387+207_1387+209dup	NP_694881.1:n.1387+207_1387+209dup
XM_011542798.1:c.1522+72_1523-74dup	XP_011541100.1:n.1522+72_1523-74dup
NM_006597.6:c.1522+72_1523-74dup MANE Select	NP_006588.1:n.1522+72_1523-74dup
NM_153201.4:c.1387+207_1387+209dup	NP_694881.1:n.1387+207_1387+209dup