Canonical Allele Identifier: CA449806667
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31785039C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817262C>G , CM000668.2:g.31817262C>G GRCh38
NC_000006.11:g.31785039C>G , CM000668.1:g.31785039C>G GRCh37
NC_000006.10:g.31893018C>G NCBI36
NG_011855.1:g.2797G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1506C>G (HSPA1A) MANE Select ENSP00000364802.5:p.Thr502=
ENST00000375651.6:c.1506C>G (HSPA1A) ENSP00000364802.5:p.Thr502=
ENST00000608703.1:c.1011C>G (HSPA1A) ENSP00000477378.1:p.Thr337=
NM_005345.5:c.1506C>G (HSPA1A) NP_005336.3:p.Thr502=
XM_005249073.2:c.-14+3751G>C (HSPA1L) XP_005249130.1:n.-14+3751G>C
XM_011514566.1:c.-14+3751G>C (HSPA1L) XP_011512868.1:n.-14+3751G>C
NM_005345.6:c.1506C>G (HSPA1A) MANE Select NP_005336.3:p.Thr502=
Search 100 bp 5'
Search 100 bp 3'