Canonical Allele Identifier: CA363409757
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31784189T>C (hg19) chr6:g.31816412T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31816412T>C , CM000668.2:g.31816412T>C GRCh38
NC_000006.11:g.31784189T>C , CM000668.1:g.31784189T>C GRCh37
NC_000006.10:g.31892168T>C NCBI36
NG_011855.1:g.3647A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.656T>C (HSPA1A) MANE Select ENSP00000364802.5:p.Val219Ala
ENST00000375651.6:c.656T>C (HSPA1A) ENSP00000364802.5:p.Val219Ala
ENST00000608703.1:c.161T>C (HSPA1A) ENSP00000477378.1:p.Val54Ala
NM_005345.5:c.656T>C (HSPA1A) NP_005336.3:p.Val219Ala
XM_005249073.2:c.-13-4427A>G (HSPA1L) XP_005249130.1:n.-13-4427A>G
XM_011514566.1:c.-13-4427A>G (HSPA1L) XP_011512868.1:n.-13-4427A>G
NM_005345.6:c.656T>C (HSPA1A) MANE Select NP_005336.3:p.Val219Ala
Search 100 bp 5'
Search 100 bp 3'