Canonical Allele Identifier: CA363417937
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31784921G>T (hg19) chr6:g.31817144G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817144G>T , CM000668.2:g.31817144G>T GRCh38
NC_000006.11:g.31784921G>T , CM000668.1:g.31784921G>T GRCh37
NC_000006.10:g.31892900G>T NCBI36
NG_011855.1:g.2915C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1388G>T (HSPA1A) MANE Select ENSP00000364802.5:p.Gly463Val
ENST00000375651.6:c.1388G>T (HSPA1A) ENSP00000364802.5:p.Gly463Val
ENST00000608703.1:c.893G>T (HSPA1A) ENSP00000477378.1:p.Gly298Val
NM_005345.5:c.1388G>T (HSPA1A) NP_005336.3:p.Gly463Val
XM_005249073.2:c.-14+3869C>A (HSPA1L) XP_005249130.1:n.-14+3869C>A
XM_011514566.1:c.-14+3869C>A (HSPA1L) XP_011512868.1:n.-14+3869C>A
NM_005345.6:c.1388G>T (HSPA1A) MANE Select NP_005336.3:p.Gly463Val
Search 100 bp 5'
Search 100 bp 3'