Canonical Allele Identifier: CA1938847762

Gene: HSPA12A

Genomic Alleles

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

Transcript Alleles

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