Canonical Allele Identifier: CA566692223

Gene: HSPA1A HSPA1L

Linked Data

• dbSNP Id: rs1353192389
• gnomAD v2: 6-31784667-C-CGT
• gnomAD v4: 6-31816890-C-CGT
• MyVariant Identifiers: chr6:g.31784667_31784668insGT (hg19) ; chr6:g.31816890_31816891insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816890_31816891insGT , CM000668.2:g.31816890_31816891insGT	GRCh38
NC_000006.11:g.31784667_31784668insGT , CM000668.1:g.31784667_31784668insGT	GRCh37
NC_000006.10:g.31892646_31892647insGT	NCBI36
NG_011855.1:g.3168_3169insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1134_1135insGT (HSPA1A) MANE Select	ENSP00000364802.5:p.Ile379ValfsTer3
ENST00000375651.6:c.1134_1135insGT (HSPA1A)	ENSP00000364802.5:p.Ile379ValfsTer3
ENST00000608703.1:c.639_640insGT (HSPA1A)	ENSP00000477378.1:p.Ile214ValfsTer3
NM_005345.5:c.1134_1135insGT (HSPA1A)	NP_005336.3:p.Ile379ValfsTer3
XM_005249073.2:c.-14+4122_-14+4123insAC (HSPA1L)	XP_005249130.1:n.-14+4122_-14+4123insAC
XM_011514566.1:c.-14+4122_-14+4123insAC (HSPA1L)	XP_011512868.1:n.-14+4122_-14+4123insAC
NM_005345.6:c.1134_1135insGT (HSPA1A) MANE Select	NP_005336.3:p.Ile379ValfsTer3