Canonical Allele Identifier: CA2691675871

Gene: HSPA5

Linked Data

• gnomAD v4: 9-125238851-T-TAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238851_125238852insAAC , CM000671.2:g.125238851_125238852insAAC	GRCh38
NC_000009.11:g.128001130_128001131insAAC , CM000671.1:g.128001130_128001131insAAC	GRCh37
NC_000009.10:g.127040951_127040952insAAC	NCBI36
NG_027761.1:g.7536_7537insGTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-25_997-24insGTT MANE Select	ENSP00000324173.6:n.997-25_997-24insGTT
ENST00000679355.1:n.1327_1328insGTT
ENST00000679475.1:n.1581-25_1581-24insGTT
ENST00000680032.1:c.997-25_997-24insGTT	ENSP00000506285.1:n.997-25_997-24insGTT
ENST00000680234.1:n.1253-25_1253-24insGTT
ENST00000680257.1:n.1253-25_1253-24insGTT
ENST00000680272.1:c.996+89_996+90insGTT	ENSP00000506097.1:n.996+89_996+90insGTT
ENST00000680494.1:n.2396_2397insGTT
ENST00000680640.1:n.1948-25_1948-24insGTT
ENST00000681045.1:n.1877-25_1877-24insGTT
ENST00000681424.1:n.1327_1328insGTT
ENST00000681540.1:n.1253-25_1253-24insGTT
ENST00000681544.1:n.1328-25_1328-24insGTT
ENST00000681675.1:n.1877-25_1877-24insGTT
ENST00000681774.1:n.2219-25_2219-24insGTT
ENST00000324460.6:c.997-25_997-24insGTT	ENSP00000324173.6:n.997-25_997-24insGTT
NM_005347.4:c.997-25_997-24insGTT	NP_005338.1:n.997-25_997-24insGTT
NM_005347.5:c.997-25_997-24insGTT MANE Select	NP_005338.1:n.997-25_997-24insGTT