Canonical Allele Identifier: CA3724184

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1043618
• ExAC: 6:31783507 G / T
• gnomAD v2: 6-31783507-G-T
• gnomAD v3: 6-31815730-G-T
• gnomAD v4: 6-31815730-G-T
• MyVariant Identifiers: chr6:g.31783507G>T (hg19) ; chr6:g.31783507_31783509delinsTGA (hg19) ; chr6:g.31815730G>T (hg38) ; chr6:g.31815730_31815732delinsTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31815730G>T , CM000668.2:g.31815730G>T	GRCh38
NC_000006.11:g.31783507G>T , CM000668.1:g.31783507G>T	GRCh37
NC_000006.10:g.31891486G>T	NCBI36
NG_011855.1:g.4329C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375651.7:c.-27G>T (HSPA1A) MANE Select	ENSP00000364802.5:n.-27G>T
ENST00000375651.6:c.-27G>T (HSPA1A)	ENSP00000364802.5:n.-27G>T
ENST00000608703.1:c.-27G>T (HSPA1A)	ENSP00000477378.1:n.-27G>T
NM_005345.5:c.-27G>T (HSPA1A)	NP_005336.3:n.-27G>T
XM_005249073.2:c.-13-3745C>A (HSPA1L)	XP_005249130.1:n.-13-3745C>A
XM_011514566.1:c.-13-3745C>A (HSPA1L)	XP_011512868.1:n.-13-3745C>A
NM_005345.6:c.-27G>T (HSPA1A) MANE Select	NP_005336.3:n.-27G>T