Canonical Allele Identifier: CA2683408035
Gene: HSPB1 HGNC NCBI

Linked Data

gnomAD v4: 7-76303698-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.76303698C>T , CM000669.2:g.76303698C>T GRCh38
NC_000007.13:g.75933015C>T , CM000669.1:g.75933015C>T GRCh37
NC_000007.12:g.75770951C>T NCBI36
NG_008995.1:g.6141C>T , LRG_248:g.6141C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248553.7:c.365-104C>T MANE Select ENSP00000248553.6:n.365-104C>T
ENST00000674547.1:c.365-104C>T ENSP00000502461.1:n.365-104C>T
ENST00000674638.1:c.365-109C>T ENSP00000502651.1:n.365-109C>T
ENST00000674650.1:c.365-286C>T ENSP00000501628.1:n.365-286C>T
ENST00000674965.1:c.365-79C>T ENSP00000501765.1:n.365-79C>T
ENST00000675134.1:c.365-104C>T ENSP00000501831.1:n.365-104C>T
ENST00000675226.1:c.369-109C>T ENSP00000502510.1:n.369-109C>T
ENST00000675417.1:n.494C>T
ENST00000675538.1:c.400-104C>T ENSP00000502495.1:n.400-104C>T
ENST00000675733.1:n.405-64C>T
ENST00000675906.1:c.365-104C>T ENSP00000502714.1:n.365-104C>T
ENST00000676195.1:n.80+42C>T
ENST00000676231.1:c.365C>T ENSP00000502249.1:p.Ala122Val
ENST00000248553.6:c.365-104C>T ENSP00000248553.6:n.365-104C>T
ENST00000429938.1:c.-170C>T ENSP00000405285.1:n.-170C>T
ENST00000447574.1:c.*425C>T ENSP00000414357.1:n.*425C>T
NM_001540.3:c.365-104C>T , LRG_248t1:c.365-104C>T NP_001531.1:n.365-104C>T
NM_001540.4:c.365-104C>T NP_001531.1:n.365-104C>T
NM_001540.5:c.365-104C>T MANE Select NP_001531.1:n.365-104C>T