Canonical Allele Identifier: CA2720660524

Gene: HSPA5

Linked Data

• dbSNP Id: rs2131453993

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.125238868_125238876dup , CM000671.2:g.125238868_125238876dup	GRCh38
NC_000009.11:g.128001147_128001155dup , CM000671.1:g.128001147_128001155dup	GRCh37
NC_000009.10:g.127040968_127040976dup	NCBI36
NG_027761.1:g.7513_7521dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000324460.7:c.997-48_997-40dup MANE Select	ENSP00000324173.6:n.997-48_997-40dup
ENST00000679355.1:n.1304_1312dup
ENST00000679475.1:n.1581-48_1581-40dup
ENST00000680032.1:c.997-48_997-40dup	ENSP00000506285.1:n.997-48_997-40dup
ENST00000680234.1:n.1253-48_1253-40dup
ENST00000680257.1:n.1253-48_1253-40dup
ENST00000680272.1:c.996+66_996+74dup	ENSP00000506097.1:n.996+66_996+74dup
ENST00000680494.1:n.2373_2381dup
ENST00000680640.1:n.1948-48_1948-40dup
ENST00000681045.1:n.1877-48_1877-40dup
ENST00000681424.1:n.1304_1312dup
ENST00000681540.1:n.1253-48_1253-40dup
ENST00000681544.1:n.1328-48_1328-40dup
ENST00000681675.1:n.1877-48_1877-40dup
ENST00000681774.1:n.2219-48_2219-40dup
ENST00000324460.6:c.997-48_997-40dup	ENSP00000324173.6:n.997-48_997-40dup
NM_005347.4:c.997-48_997-40dup	NP_005338.1:n.997-48_997-40dup
NM_005347.5:c.997-48_997-40dup MANE Select	NP_005338.1:n.997-48_997-40dup