Canonical Allele Identifier: CA16403235
Gene: HSPA12A HGNC NCBI

Linked Data

dbSNP Id: rs1665650

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.116727589T>C , CM000672.2:g.116727589T>C GRCh38
NC_000010.10:g.118487100T>C , CM000672.1:g.118487100T>C GRCh37
NC_000010.9:g.118477090T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369209.8:c.40+14841A>G MANE Select ENSP00000358211.3:n.40+14841A>G
ENST00000481291.2:n.166+14841A>G
ENST00000635765.1:c.92-20304A>G ENSP00000489674.1:n.92-20304A>G
ENST00000674167.1:c.-123-22311A>G ENSP00000501417.1:n.-123-22311A>G
ENST00000674197.1:c.89-20304A>G ENSP00000501472.1:n.89-20304A>G
ENST00000674205.1:c.40+14841A>G ENSP00000501491.1:n.40+14841A>G
ENST00000674344.1:c.-97+14841A>G ENSP00000501346.1:n.-97+14841A>G
ENST00000674347.1:c.40+14841A>G ENSP00000501463.1:n.40+14841A>G
ENST00000674372.1:n.73+14417A>G
ENST00000674394.1:c.40+14841A>G ENSP00000501506.1:n.40+14841A>G
ENST00000674401.1:c.-209-20304A>G ENSP00000501414.1:n.-209-20304A>G
ENST00000674459.1:c.-124+14841A>G ENSP00000501445.1:n.-124+14841A>G
ENST00000674491.1:c.40+14841A>G ENSP00000501460.1:n.40+14841A>G
ENST00000674505.1:c.-209-20304A>G ENSP00000501396.1:n.-209-20304A>G
ENST00000369209.7:c.40+14841A>G ENSP00000358211.3:n.40+14841A>G
NM_025015.2:c.40+14841A>G NP_079291.2:n.40+14841A>G
XM_005269672.2:c.92-20304A>G XP_005269729.1:n.92-20304A>G
XM_005269673.3:c.89-20304A>G XP_005269730.1:n.89-20304A>G
XM_011539579.1:c.89-20304A>G XP_011537881.1:n.89-20304A>G
XM_011539580.1:c.-363-209A>G XP_011537882.1:n.-363-209A>G
NM_001330164.1:c.92-20304A>G NP_001317093.1:n.92-20304A>G
XM_005269673.5:c.89-20304A>G XP_005269730.1:n.89-20304A>G
XM_011539579.2:c.89-20304A>G XP_011537881.1:n.89-20304A>G
XM_011539580.2:c.-363-209A>G XP_011537882.1:n.-363-209A>G
XM_017016032.2:c.-197+14841A>G XP_016871521.1:n.-197+14841A>G
NM_001330164.2:c.92-20304A>G NP_001317093.1:n.92-20304A>G
NM_025015.3:c.40+14841A>G MANE Select NP_079291.2:n.40+14841A>G