Canonical Allele Identifier: CA363418872
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31784995G>T (hg19) chr6:g.31817218G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817218G>T , CM000668.2:g.31817218G>T GRCh38
NC_000006.11:g.31784995G>T , CM000668.1:g.31784995G>T GRCh37
NC_000006.10:g.31892974G>T NCBI36
NG_011855.1:g.2841C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1462G>T (HSPA1A) MANE Select ENSP00000364802.5:p.Val488Phe
ENST00000375651.6:c.1462G>T (HSPA1A) ENSP00000364802.5:p.Val488Phe
ENST00000608703.1:c.967G>T (HSPA1A) ENSP00000477378.1:p.Val323Phe
NM_005345.5:c.1462G>T (HSPA1A) NP_005336.3:p.Val488Phe
XM_005249073.2:c.-14+3795C>A (HSPA1L) XP_005249130.1:n.-14+3795C>A
XM_011514566.1:c.-14+3795C>A (HSPA1L) XP_011512868.1:n.-14+3795C>A
NM_005345.6:c.1462G>T (HSPA1A) MANE Select NP_005336.3:p.Val488Phe
Search 100 bp 5'
Search 100 bp 3'