Canonical Allele Identifier: CA1938862198

Gene: HSPA12A

Genomic Alleles

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

Transcript Alleles

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