Canonical Allele Identifier: CA449805847
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1554231727
MyVariant Identifiers: chr6:g.31784211C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816434C>T , CM000668.2:g.31816434C>T GRCh38
NC_000006.11:g.31784211C>T , CM000668.1:g.31784211C>T GRCh37
NC_000006.10:g.31892190C>T NCBI36
NG_011855.1:g.3625G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.678C>T (HSPA1A) MANE Select ENSP00000364802.5:p.Thr226=
ENST00000375651.6:c.678C>T (HSPA1A) ENSP00000364802.5:p.Thr226=
ENST00000608703.1:c.183C>T (HSPA1A) ENSP00000477378.1:p.Thr61=
NM_005345.5:c.678C>T (HSPA1A) NP_005336.3:p.Thr226=
XM_005249073.2:c.-13-4449G>A (HSPA1L) XP_005249130.1:n.-13-4449G>A
XM_011514566.1:c.-13-4449G>A (HSPA1L) XP_011512868.1:n.-13-4449G>A
NM_005345.6:c.678C>T (HSPA1A) MANE Select NP_005336.3:p.Thr226=
Search 100 bp 5'
Search 100 bp 3'