Canonical Allele Identifier: CA2605324178

Gene: ABLIM3

Linked Data

• dbSNP Id: rs2127493690
• gnomAD v3: 5-149196603-C-T
• gnomAD v4: 5-149196603-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.149196603C>T , CM000667.2:g.149196603C>T	GRCh38
NC_000005.9:g.148576166C>T , CM000667.1:g.148576166C>T	GRCh37
NC_000005.8:g.148556359C>T	NCBI36
NG_051566.1:g.60157C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309868.12:c.152-1616C>T MANE Select	ENSP00000310309.7:n.152-1616C>T
ENST00000309868.11:c.152-1616C>T	ENSP00000310309.7:n.152-1616C>T
ENST00000326685.11:c.152-1616C>T	ENSP00000315841.7:n.152-1616C>T
ENST00000504238.5:c.152-1616C>T	ENSP00000421183.1:n.152-1616C>T
ENST00000506113.5:c.152-1616C>T	ENSP00000425394.1:n.152-1616C>T
ENST00000508983.5:c.152-1616C>T	ENSP00000420855.1:n.152-1616C>T
ENST00000515171.5:c.152-1616C>T	ENSP00000421002.1:n.152-1616C>T
ENST00000515796.1:n.42-1616C>T
NM_001301015.1:c.152-1616C>T	NP_001287944.1:n.152-1616C>T
NM_001301018.1:c.152-1616C>T	NP_001287947.1:n.152-1616C>T
NM_001301027.1:c.97-1616C>T	NP_001287956.1:n.97-1616C>T
NM_001301028.1:c.152-1616C>T	NP_001287957.1:n.152-1616C>T
NM_014945.3:c.152-1616C>T	NP_055760.1:n.152-1616C>T
XM_005268392.1:c.152-1616C>T	XP_005268449.1:n.152-1616C>T
XM_005268393.1:c.152-1616C>T	XP_005268450.1:n.152-1616C>T
XM_005268394.1:c.152-1616C>T	XP_005268451.1:n.152-1616C>T
XM_005268395.1:c.152-1616C>T	XP_005268452.1:n.152-1616C>T
XM_005268396.1:c.152-1616C>T	XP_005268453.1:n.152-1616C>T
XM_011537609.1:c.152-1616C>T	XP_011535911.1:n.152-1616C>T
NM_001301015.2:c.152-1616C>T	NP_001287944.1:n.152-1616C>T
NM_001301018.2:c.152-1616C>T	NP_001287947.1:n.152-1616C>T
NM_001301027.2:c.97-1616C>T	NP_001287956.1:n.97-1616C>T
NM_001301028.2:c.152-1616C>T	NP_001287957.1:n.152-1616C>T
NM_001345858.1:c.152-1616C>T	NP_001332787.1:n.152-1616C>T
NM_001345859.1:c.152-1616C>T	NP_001332788.1:n.152-1616C>T
NM_001345860.1:c.152-1616C>T	NP_001332789.1:n.152-1616C>T
NM_001345861.1:c.152-1616C>T	NP_001332790.1:n.152-1616C>T
NM_014945.4:c.152-1616C>T	NP_055760.1:n.152-1616C>T
XM_005268394.2:c.152-1616C>T	XP_005268451.1:n.152-1616C>T
XM_011537609.3:c.152-1616C>T	XP_011535911.1:n.152-1616C>T
XM_024446003.1:c.152-1616C>T	XP_024301771.1:n.152-1616C>T
XM_024446004.1:c.152-1616C>T	XP_024301772.1:n.152-1616C>T
XM_024446005.1:c.152-1616C>T	XP_024301773.1:n.152-1616C>T
XM_024446006.1:c.152-1616C>T	XP_024301774.1:n.152-1616C>T
NM_001301015.3:c.152-1616C>T	NP_001287944.1:n.152-1616C>T
NM_001301028.3:c.152-1616C>T	NP_001287957.1:n.152-1616C>T
NM_001345861.2:c.152-1616C>T	NP_001332790.1:n.152-1616C>T
NM_001370417.1:c.152-1616C>T	NP_001357346.1:n.152-1616C>T
NM_001370418.1:c.152-1616C>T	NP_001357347.1:n.152-1616C>T
NM_001301018.3:c.152-1616C>T	NP_001287947.1:n.152-1616C>T
NM_001345858.2:c.152-1616C>T	NP_001332787.1:n.152-1616C>T
NM_001345859.2:c.152-1616C>T	NP_001332788.1:n.152-1616C>T
NM_001345860.2:c.152-1616C>T	NP_001332789.1:n.152-1616C>T
NM_014945.5:c.152-1616C>T MANE Select	NP_055760.1:n.152-1616C>T