Canonical Allele Identifier: CA468969779

Gene: ANKRD30A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.37219522A>T , CM000672.2:g.37219522A>T	GRCh38
NC_000010.10:g.37508450A>T , CM000672.1:g.37508450A>T	GRCh37
NC_000010.9:g.37548456A>T	NCBI36
NG_051556.1:g.98781A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696674.1:c.543A>T	ENSP00000512798.1:p.Ala181=
ENST00000361713.2:c.3810A>T MANE Select	ENSP00000354432.2:p.Ala1270=
ENST00000374660.7:c.4167A>T	ENSP00000363792.2:p.Ala1389=
ENST00000602533.7:c.3810A>T	ENSP00000473551.2:p.Ala1270=
ENST00000374660.6:c.4167A>T	ENSP00000363792.2:p.Ala1389=
ENST00000602533.6:c.3810A>T	ENSP00000473551.2:p.Ala1270=
ENST00000361713.1:c.3642A>T	ENSP00000354432.1:p.Ala1214=
ENST00000374660.5:c.3999A>T	ENSP00000363792.1:p.Ala1333=
ENST00000602533.5:c.3642A>T	ENSP00000473551.1:p.Ala1214=
ENST00000611781.4:c.3810A>T	ENSP00000477963.1:p.Ala1270=
NM_052997.2:c.3642A>T	NP_443723.2:p.Ala1214=
XM_011519757.1:c.4251A>T	XP_011518059.1:p.Ala1417=
XR_930524.1:n.4297A>T
XM_011519757.3:c.4251A>T	XP_011518059.1:p.Ala1417=
XM_011519758.2:c.*488A>T	XP_011518060.1:n.*488A>T
XM_017016883.2:c.1971A>T	XP_016872372.1:p.Ala657=
XR_001747257.1:n.4285A>T
XR_002957039.1:n.4285A>T
XR_002957040.1:n.4285A>T
XR_002957041.1:n.4285A>T
XR_002957042.1:n.4285A>T
XR_002957043.1:n.4285A>T
XR_002957044.1:n.4285A>T
XR_002957045.1:n.4285A>T
XR_002957046.1:n.4285A>T
XR_002957047.1:n.4285A>T
XR_002957048.1:n.4285A>T
XR_930524.3:n.4285A>T
NM_052997.3:c.3810A>T MANE Select	NP_443723.3:p.Ala1270=