Canonical Allele Identifier: CA2678043797

Gene: HSPA1A HSPA1L

Linked Data

• gnomAD v4: 6-31816619-T-TAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816619_31816620insAA , CM000668.2:g.31816619_31816620insAA	GRCh38
NC_000006.11:g.31784396_31784397insAA , CM000668.1:g.31784396_31784397insAA	GRCh37
NC_000006.10:g.31892375_31892376insAA	NCBI36
NG_011855.1:g.3439_3440insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.863_864insAA (HSPA1A) MANE Select	ENSP00000364802.5:p.Phe288LeufsTer?
ENST00000375651.6:c.863_864insAA (HSPA1A)	ENSP00000364802.5:p.Phe288LeufsTer?
ENST00000608703.1:c.368_369insAA (HSPA1A)	ENSP00000477378.1:p.Phe123LeufsTer?
NM_005345.5:c.863_864insAA (HSPA1A)	NP_005336.3:p.Phe288LeufsTer?
XM_005249073.2:c.-14+4393_-14+4394insTT (HSPA1L)	XP_005249130.1:n.-14+4393_-14+4394insTT
XM_011514566.1:c.-14+4393_-14+4394insTT (HSPA1L)	XP_011512868.1:n.-14+4393_-14+4394insTT
NM_005345.6:c.863_864insAA (HSPA1A) MANE Select	NP_005336.3:p.Phe288LeufsTer?