Canonical Allele Identifier: CA363410569
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31784254T>A (hg19) chr6:g.31816477T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816477T>A , CM000668.2:g.31816477T>A GRCh38
NC_000006.11:g.31784254T>A , CM000668.1:g.31784254T>A GRCh37
NC_000006.10:g.31892233T>A NCBI36
NG_011855.1:g.3582A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.721T>A (HSPA1A) MANE Select ENSP00000364802.5:p.Phe241Ile
ENST00000375651.6:c.721T>A (HSPA1A) ENSP00000364802.5:p.Phe241Ile
ENST00000608703.1:c.226T>A (HSPA1A) ENSP00000477378.1:p.Phe76Ile
NM_005345.5:c.721T>A (HSPA1A) NP_005336.3:p.Phe241Ile
XM_005249073.2:c.-13-4492A>T (HSPA1L) XP_005249130.1:n.-13-4492A>T
XM_011514566.1:c.-13-4492A>T (HSPA1L) XP_011512868.1:n.-13-4492A>T
NM_005345.6:c.721T>A (HSPA1A) MANE Select NP_005336.3:p.Phe241Ile
Search 100 bp 5'
Search 100 bp 3'