Canonical Allele Identifier: CA350204250

Gene: HSPD1

Linked Data

• gnomAD v4: 2-197498773-A-G
• MyVariant Identifiers: chr2:g.198363497A>G (hg19) ; chr2:g.197498773A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197498773A>G , CM000664.2:g.197498773A>G	GRCh38
NC_000002.11:g.198363497A>G , CM000664.1:g.198363497A>G	GRCh37
NC_000002.10:g.198071742A>G	NCBI36
NG_008914.1:g.3777A>G
NG_008915.1:g.6502T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388968.8:c.76T>C MANE Select	ENSP00000373620.3:p.Tyr26His
ENST00000418022.2:c.76T>C	ENSP00000412227.2:p.Tyr26His
ENST00000426480.2:c.76T>C	ENSP00000414446.2:p.Tyr26His
ENST00000428204.6:c.76T>C	ENSP00000396460.2:p.Tyr26His
ENST00000430176.6:c.76T>C	ENSP00000393670.2:p.Tyr26His
ENST00000439605.2:c.76T>C	ENSP00000402478.2:p.Tyr26His
ENST00000440114.2:c.76T>C	ENSP00000390404.1:p.Tyr26His
ENST00000452200.6:c.76T>C	ENSP00000412717.2:p.Tyr26His
ENST00000461097.2:n.114T>C
ENST00000476746.6:n.177T>C
ENST00000676933.1:c.76T>C	ENSP00000503144.1:p.Tyr26His
ENST00000677403.1:c.76T>C	ENSP00000504667.1:p.Tyr26His
ENST00000677454.1:c.76T>C	ENSP00000503295.1:p.Tyr26His
ENST00000677792.1:c.76T>C	ENSP00000504645.1:p.Tyr26His
ENST00000677913.1:c.76T>C	ENSP00000503139.1:p.Tyr26His
ENST00000678170.1:c.76T>C	ENSP00000503910.1:p.Tyr26His
ENST00000678545.1:c.76T>C	ENSP00000502920.1:p.Tyr26His
ENST00000678621.1:c.76T>C	ENSP00000504328.1:p.Tyr26His
ENST00000678761.1:c.76T>C	ENSP00000503894.1:p.Tyr26His
ENST00000678969.1:n.176T>C
ENST00000679291.1:c.76T>C	ENSP00000504417.1:p.Tyr26His
ENST00000345042.6:c.76T>C	ENSP00000340019.2:p.Tyr26His
ENST00000388968.7:c.76T>C	ENSP00000373620.3:p.Tyr26His
ENST00000418022.1:c.76T>C	ENSP00000412227.1:p.Tyr26His
ENST00000426480.1:c.202T>C	ENSP00000414446.1:p.Tyr68His
ENST00000428204.5:c.76T>C	ENSP00000396460.1:p.Tyr26His
ENST00000430176.5:c.76T>C	ENSP00000393670.1:p.Tyr26His
ENST00000439605.1:c.76T>C	ENSP00000402478.1:p.Tyr26His
ENST00000440114.1:c.76T>C	ENSP00000390404.1:p.Tyr26His
ENST00000452200.5:c.76T>C	ENSP00000412717.1:p.Tyr26His
ENST00000461097.1:n.114T>C
ENST00000476746.5:n.176T>C
NM_002156.4:c.76T>C	NP_002147.2:p.Tyr26His
NM_199440.1:c.76T>C	NP_955472.1:p.Tyr26His
XM_005246518.2:c.76T>C	XP_005246575.1:p.Tyr26His
NM_002156.5:c.76T>C MANE Select	NP_002147.2:p.Tyr26His
NM_199440.2:c.76T>C	NP_955472.1:p.Tyr26His