Canonical Allele Identifier: CA538526737

Gene: HSPD1

Linked Data

• dbSNP Id: rs1314058809
• gnomAD v2: 2-198360829-C-CAGA
• gnomAD v3: 2-197496105-C-CAGA
• gnomAD v4: 2-197496105-C-CAGA
• MyVariant Identifiers: chr2:g.198360829_198360830insAGA (hg19) ; chr2:g.197496105_197496106insAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.197496105_197496106insAGA , CM000664.2:g.197496105_197496106insAGA	GRCh38
NC_000002.11:g.198360829_198360830insAGA , CM000664.1:g.198360829_198360830insAGA	GRCh37
NC_000002.10:g.198069074_198069075insAGA	NCBI36
NG_008914.1:g.1109_1110insAGA
NG_008915.1:g.9169_9170insTCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000388968.8:c.428-730_428-729insTCT MANE Select	ENSP00000373620.3:n.428-730_428-729insTCT
ENST00000418022.2:c.428-730_428-729insTCT	ENSP00000412227.2:n.428-730_428-729insTCT
ENST00000426480.2:c.428-730_428-729insTCT	ENSP00000414446.2:n.428-730_428-729insTCT
ENST00000428204.6:c.428-730_428-729insTCT	ENSP00000396460.2:n.428-730_428-729insTCT
ENST00000430176.6:c.428-730_428-729insTCT	ENSP00000393670.2:n.428-730_428-729insTCT
ENST00000439605.2:c.428-730_428-729insTCT	ENSP00000402478.2:n.428-730_428-729insTCT
ENST00000440114.2:c.*234-730_*234-729insTCT	ENSP00000390404.1:n.*234-730_*234-729insTCT
ENST00000452200.6:c.428-730_428-729insTCT	ENSP00000412717.2:n.428-730_428-729insTCT
ENST00000461097.2:n.1499_1500insTCT
ENST00000476746.6:n.529-730_529-729insTCT
ENST00000676933.1:c.428-730_428-729insTCT	ENSP00000503144.1:n.428-730_428-729insTCT
ENST00000677403.1:c.428-730_428-729insTCT	ENSP00000504667.1:n.428-730_428-729insTCT
ENST00000677454.1:c.428-730_428-729insTCT	ENSP00000503295.1:n.428-730_428-729insTCT
ENST00000677792.1:c.428-730_428-729insTCT	ENSP00000504645.1:n.428-730_428-729insTCT
ENST00000677913.1:c.428-730_428-729insTCT	ENSP00000503139.1:n.428-730_428-729insTCT
ENST00000678170.1:c.427+1034_427+1035insTCT	ENSP00000503910.1:n.427+1034_427+1035insTCT
ENST00000678545.1:c.428-730_428-729insTCT	ENSP00000502920.1:n.428-730_428-729insTCT
ENST00000678621.1:c.428-730_428-729insTCT	ENSP00000504328.1:n.428-730_428-729insTCT
ENST00000678761.1:c.428-730_428-729insTCT	ENSP00000503894.1:n.428-730_428-729insTCT
ENST00000678969.1:n.528-730_528-729insTCT
ENST00000679291.1:c.428-730_428-729insTCT	ENSP00000504417.1:n.428-730_428-729insTCT
ENST00000345042.6:c.428-730_428-729insTCT	ENSP00000340019.2:n.428-730_428-729insTCT
ENST00000388968.7:c.428-730_428-729insTCT	ENSP00000373620.3:n.428-730_428-729insTCT
ENST00000430176.5:c.428-730_428-729insTCT	ENSP00000393670.1:n.428-730_428-729insTCT
ENST00000440114.1:c.*234-730_*234-729insTCT	ENSP00000390404.1:n.*234-730_*234-729insTCT
ENST00000452200.5:c.428-730_428-729insTCT	ENSP00000412717.1:n.428-730_428-729insTCT
ENST00000476746.5:n.528-730_528-729insTCT
ENST00000486181.5:n.369-730_369-729insTCT
NM_002156.4:c.428-730_428-729insTCT	NP_002147.2:n.428-730_428-729insTCT
NM_199440.1:c.428-730_428-729insTCT	NP_955472.1:n.428-730_428-729insTCT
XM_005246518.2:c.428-730_428-729insTCT	XP_005246575.1:n.428-730_428-729insTCT
NM_002156.5:c.428-730_428-729insTCT MANE Select	NP_002147.2:n.428-730_428-729insTCT
NM_199440.2:c.428-730_428-729insTCT	NP_955472.1:n.428-730_428-729insTCT