Canonical Allele Identifier: CA367765563
Gene: HSPB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303858A>G , CM000669.2:g.76303858A>G GRCh38
NC_000007.13:g.75933175A>G , CM000669.1:g.75933175A>G GRCh37
NC_000007.12:g.75771111A>G NCBI36
NG_008995.1:g.6301A>G , LRG_248:g.6301A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.421A>G MANE Select ENSP00000248553.6:p.Lys141Glu
ENST00000674547.1:c.421A>G ENSP00000502461.1:p.Lys141Glu
ENST00000674638.1:c.416A>G ENSP00000502651.1:p.Glu139Gly
ENST00000674650.1:c.365-126A>G ENSP00000501628.1:n.365-126A>G
ENST00000674965.1:c.*77A>G ENSP00000501765.1:n.*77A>G
ENST00000675134.1:c.407+14A>G ENSP00000501831.1:n.407+14A>G
ENST00000675226.1:c.420A>G ENSP00000502510.1:p.Gly140=
ENST00000675417.1:n.654A>G
ENST00000675538.1:c.456A>G ENSP00000502495.1:p.Gly152=
ENST00000675906.1:c.421A>G ENSP00000502714.1:p.Lys141Glu
ENST00000676195.1:n.137A>G
ENST00000676231.1:c.451A>G ENSP00000502249.1:p.Lys151Glu
ENST00000248553.6:c.421A>G ENSP00000248553.6:p.Lys141Glu
ENST00000429938.1:c.-84A>G ENSP00000405285.1:n.-84A>G
ENST00000447574.1:c.*585A>G ENSP00000414357.1:n.*585A>G
NM_001540.3:c.421A>G , LRG_248t1:c.421A>G NP_001531.1:p.Lys141Glu
NM_001540.4:c.421A>G NP_001531.1:p.Lys141Glu
NM_001540.5:c.421A>G MANE Select NP_001531.1:p.Lys141Glu