Canonical Allele Identifier: CA2678044547

Gene: HSPA1A HSPA1L

Linked Data

• gnomAD v4: 6-31816860-T-TCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31816860_31816861insCG , CM000668.2:g.31816860_31816861insCG	GRCh38
NC_000006.11:g.31784637_31784638insCG , CM000668.1:g.31784637_31784638insCG	GRCh37
NC_000006.10:g.31892616_31892617insCG	NCBI36
NG_011855.1:g.3198_3199insCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375651.7:c.1104_1105insCG (HSPA1A) MANE Select	ENSP00000364802.5:p.Val369ArgfsTer13
ENST00000375651.6:c.1104_1105insCG (HSPA1A)	ENSP00000364802.5:p.Val369ArgfsTer13
ENST00000608703.1:c.609_610insCG (HSPA1A)	ENSP00000477378.1:p.Val204ArgfsTer13
NM_005345.5:c.1104_1105insCG (HSPA1A)	NP_005336.3:p.Val369ArgfsTer13
XM_005249073.2:c.-14+4152_-14+4153insCG (HSPA1L)	XP_005249130.1:n.-14+4152_-14+4153insCG
XM_011514566.1:c.-14+4152_-14+4153insCG (HSPA1L)	XP_011512868.1:n.-14+4152_-14+4153insCG
NM_005345.6:c.1104_1105insCG (HSPA1A) MANE Select	NP_005336.3:p.Val369ArgfsTer13