Canonical Allele Identifier: CA660416531
Gene: HSPA12A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.116695732C>G , CM000672.2:g.116695732C>G GRCh38
NC_000010.10:g.118455243C>G , CM000672.1:g.118455243C>G GRCh37
NC_000010.9:g.118445233C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369209.8:c.546+2903G>C MANE Select ENSP00000358211.3:n.546+2903G>C
ENST00000635765.1:c.597+2903G>C ENSP00000489674.1:n.597+2903G>C
ENST00000674167.1:c.297+2903G>C ENSP00000501417.1:n.297+2903G>C
ENST00000674197.1:c.594+2903G>C ENSP00000501472.1:n.594+2903G>C
ENST00000674205.1:c.546+2903G>C ENSP00000501491.1:n.546+2903G>C
ENST00000674223.1:n.599+2903G>C
ENST00000674344.1:c.-96-3265G>C ENSP00000501346.1:n.-96-3265G>C
ENST00000674347.1:c.546+2903G>C ENSP00000501463.1:n.546+2903G>C
ENST00000674372.1:n.579+2903G>C
ENST00000674375.1:n.556+2903G>C
ENST00000674394.1:c.255-3265G>C ENSP00000501506.1:n.255-3265G>C
ENST00000674401.1:c.297+2903G>C ENSP00000501414.1:n.297+2903G>C
ENST00000674459.1:c.297+2903G>C ENSP00000501445.1:n.297+2903G>C
ENST00000674473.1:c.378+2903G>C
ENST00000674491.1:c.*503+2903G>C ENSP00000501460.1:n.*503+2903G>C
ENST00000674505.1:c.297+2903G>C ENSP00000501396.1:n.297+2903G>C
ENST00000369209.7:c.546+2903G>C ENSP00000358211.3:n.546+2903G>C
NM_025015.2:c.546+2903G>C NP_079291.2:n.546+2903G>C
XM_005269672.2:c.597+2903G>C XP_005269729.1:n.597+2903G>C
XM_005269673.3:c.594+2903G>C XP_005269730.1:n.594+2903G>C
XM_011539579.1:c.594+2903G>C XP_011537881.1:n.594+2903G>C
XM_011539580.1:c.297+2903G>C XP_011537882.1:n.297+2903G>C
XM_011539581.1:c.19-3265G>C XP_011537883.1:n.19-3265G>C
NM_001330164.1:c.597+2903G>C NP_001317093.1:n.597+2903G>C
XM_005269673.5:c.594+2903G>C XP_005269730.1:n.594+2903G>C
XM_011539579.2:c.594+2903G>C XP_011537881.1:n.594+2903G>C
XM_011539580.2:c.297+2903G>C XP_011537882.1:n.297+2903G>C
XM_017016032.2:c.19-3265G>C XP_016871521.1:n.19-3265G>C
NM_001330164.2:c.597+2903G>C NP_001317093.1:n.597+2903G>C
NM_025015.3:c.546+2903G>C MANE Select NP_079291.2:n.546+2903G>C