Canonical Allele Identifier: CA1590382358

Gene: ABLIM3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149196623T= , CM000667.2:g.149196623T=	GRCh38
NC_000005.9:g.148576186T= , CM000667.1:g.148576186T=	GRCh37
NC_000005.8:g.148556379T=	NCBI36
NG_051566.1:g.60177T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309868.12:c.152-1596T= MANE Select	ENSP00000310309.7:n.152-1596T=
ENST00000309868.11:c.152-1596T=	ENSP00000310309.7:n.152-1596T=
ENST00000326685.11:c.152-1596T=	ENSP00000315841.7:n.152-1596T=
ENST00000504238.5:c.152-1596T=	ENSP00000421183.1:n.152-1596T=
ENST00000506113.5:c.152-1596T=	ENSP00000425394.1:n.152-1596T=
ENST00000508983.5:c.152-1596T=	ENSP00000420855.1:n.152-1596T=
ENST00000515171.5:c.152-1596T=	ENSP00000421002.1:n.152-1596T=
ENST00000515796.1:n.42-1596T=
NM_001301015.1:c.152-1596T=	NP_001287944.1:n.152-1596T=
NM_001301018.1:c.152-1596T=	NP_001287947.1:n.152-1596T=
NM_001301027.1:c.97-1596T=	NP_001287956.1:n.97-1596T=
NM_001301028.1:c.152-1596T=	NP_001287957.1:n.152-1596T=
NM_014945.3:c.152-1596T=	NP_055760.1:n.152-1596T=
XM_005268392.1:c.152-1596T=	XP_005268449.1:n.152-1596T=
XM_005268393.1:c.152-1596T=	XP_005268450.1:n.152-1596T=
XM_005268394.1:c.152-1596T=	XP_005268451.1:n.152-1596T=
XM_005268395.1:c.152-1596T=	XP_005268452.1:n.152-1596T=
XM_005268396.1:c.152-1596T=	XP_005268453.1:n.152-1596T=
XM_011537609.1:c.152-1596T=	XP_011535911.1:n.152-1596T=
NM_001301015.2:c.152-1596T=	NP_001287944.1:n.152-1596T=
NM_001301018.2:c.152-1596T=	NP_001287947.1:n.152-1596T=
NM_001301027.2:c.97-1596T=	NP_001287956.1:n.97-1596T=
NM_001301028.2:c.152-1596T=	NP_001287957.1:n.152-1596T=
NM_001345858.1:c.152-1596T=	NP_001332787.1:n.152-1596T=
NM_001345859.1:c.152-1596T=	NP_001332788.1:n.152-1596T=
NM_001345860.1:c.152-1596T=	NP_001332789.1:n.152-1596T=
NM_001345861.1:c.152-1596T=	NP_001332790.1:n.152-1596T=
NM_014945.4:c.152-1596T=	NP_055760.1:n.152-1596T=
XM_005268394.2:c.152-1596T=	XP_005268451.1:n.152-1596T=
XM_011537609.3:c.152-1596T=	XP_011535911.1:n.152-1596T=
XM_024446003.1:c.152-1596T=	XP_024301771.1:n.152-1596T=
XM_024446004.1:c.152-1596T=	XP_024301772.1:n.152-1596T=
XM_024446005.1:c.152-1596T=	XP_024301773.1:n.152-1596T=
XM_024446006.1:c.152-1596T=	XP_024301774.1:n.152-1596T=
NM_001301015.3:c.152-1596T=	NP_001287944.1:n.152-1596T=
NM_001301028.3:c.152-1596T=	NP_001287957.1:n.152-1596T=
NM_001345861.2:c.152-1596T=	NP_001332790.1:n.152-1596T=
NM_001370417.1:c.152-1596T=	NP_001357346.1:n.152-1596T=
NM_001370418.1:c.152-1596T=	NP_001357347.1:n.152-1596T=
NM_001301018.3:c.152-1596T=	NP_001287947.1:n.152-1596T=
NM_001345858.2:c.152-1596T=	NP_001332787.1:n.152-1596T=
NM_001345859.2:c.152-1596T=	NP_001332788.1:n.152-1596T=
NM_001345860.2:c.152-1596T=	NP_001332789.1:n.152-1596T=
NM_014945.5:c.152-1596T= MANE Select	NP_055760.1:n.152-1596T=