Canonical Allele Identifier: CA566692203
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1233263833
gnomAD v2: 6-31785035-TCAC-T
MyVariant Identifiers: chr6:g.31785036_31785038del (hg19) chr6:g.31817259_31817261del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817261_31817263del , CM000668.2:g.31817261_31817263del GRCh38
NC_000006.11:g.31785038_31785040del , CM000668.1:g.31785038_31785040del GRCh37
NC_000006.10:g.31893017_31893019del NCBI36
NG_011855.1:g.2798_2800del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1505_1507del (HSPA1A) MANE Select ENSP00000364802.5:p.Thr502del
ENST00000375651.6:c.1505_1507del (HSPA1A) ENSP00000364802.5:p.Thr502del
ENST00000608703.1:c.1010_1012del (HSPA1A) ENSP00000477378.1:p.Thr337del
NM_005345.5:c.1505_1507del (HSPA1A) NP_005336.3:p.Thr502del
XM_005249073.2:c.-14+3752_-14+3754del (HSPA1L) XP_005249130.1:n.-14+3752_-14+3754del
XM_011514566.1:c.-14+3752_-14+3754del (HSPA1L) XP_011512868.1:n.-14+3752_-14+3754del
NM_005345.6:c.1505_1507del (HSPA1A) MANE Select NP_005336.3:p.Thr502del
Search 100 bp 5'
Search 100 bp 3'