Canonical Allele Identifier: CA449806632
Gene: HSPA1A HGNC NCBI
HSPA1L HGNC NCBI

Linked Data

dbSNP Id: rs1337131838
gnomAD v2: 6-31785018-C-G
gnomAD v3: 6-31817241-C-G
gnomAD v4: 6-31817241-C-G
MyVariant Identifiers: chr6:g.31785018C>G (hg19) chr6:g.31817241C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31817241C>G , CM000668.2:g.31817241C>G GRCh38
NC_000006.11:g.31785018C>G , CM000668.1:g.31785018C>G GRCh37
NC_000006.10:g.31892997C>G NCBI36
NG_011855.1:g.2818G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000375651.7:c.1485C>G (HSPA1A) MANE Select ENSP00000364802.5:p.Thr495=
ENST00000375651.6:c.1485C>G (HSPA1A) ENSP00000364802.5:p.Thr495=
ENST00000608703.1:c.990C>G (HSPA1A) ENSP00000477378.1:p.Thr330=
NM_005345.5:c.1485C>G (HSPA1A) NP_005336.3:p.Thr495=
XM_005249073.2:c.-14+3772G>C (HSPA1L) XP_005249130.1:n.-14+3772G>C
XM_011514566.1:c.-14+3772G>C (HSPA1L) XP_011512868.1:n.-14+3772G>C
NM_005345.6:c.1485C>G (HSPA1A) MANE Select NP_005336.3:p.Thr495=
Search 100 bp 5'
Search 100 bp 3'