Canonical Allele Identifier: CA1264634

Gene: ABL2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179108917T>A , CM000663.2:g.179108917T>A	GRCh38
NC_000001.10:g.179078052T>A , CM000663.1:g.179078052T>A	GRCh37
NC_000001.9:g.177344675T>A	NCBI36
NG_028242.1:g.125768A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_007314.4:c.2350A>T MANE Select	NP_009298.1:p.Thr784Ser
ENST00000502732.6:c.2350A>T MANE Select	ENSP00000427562.1:p.Thr784Ser
NM_001136000.2:c.2015-19A>T	NP_001129472.1:n.2015-19A>T
NM_001136000.3:c.2015-19A>T	NP_001129472.1:n.2015-19A>T
NM_001168236.1:c.2287A>T	NP_001161708.1:p.Thr763Ser
NM_001168236.2:c.2287A>T	NP_001161708.1:p.Thr763Ser
NM_001168237.1:c.2060-19A>T	NP_001161709.1:n.2060-19A>T
NM_001168237.2:c.2060-19A>T	NP_001161709.1:n.2060-19A>T
NM_001168238.1:c.1997-19A>T	NP_001161710.1:n.1997-19A>T
NM_001168238.2:c.1997-19A>T	NP_001161710.1:n.1997-19A>T
NM_001168239.1:c.1952-19A>T	NP_001161711.1:n.1952-19A>T
NM_001168239.2:c.1952-19A>T	NP_001161711.1:n.1952-19A>T
NM_005158.4:c.2305A>T	NP_005149.4:p.Thr769Ser
NM_005158.5:c.2305A>T	NP_005149.4:p.Thr769Ser
NM_007314.3:c.2350A>T	NP_009298.1:p.Thr784Ser
ENST00000344730.7:c.2015-19A>T	ENSP00000339209.3:n.2015-19A>T
ENST00000344730.8:c.2015-19A>T	ENSP00000339209.3:n.2015-19A>T
ENST00000367623.8:c.2287A>T	ENSP00000356595.4:p.Thr763Ser
ENST00000502732.5:c.2350A>T	ENSP00000427562.1:p.Thr784Ser
ENST00000504405.5:c.1952-19A>T	ENSP00000426831.1:n.1952-19A>T
ENST00000507173.5:c.1997-19A>T	ENSP00000423413.1:n.1997-19A>T
ENST00000511413.5:c.2060-19A>T	ENSP00000424697.1:n.2060-19A>T
ENST00000512653.5:c.2305A>T	ENSP00000423578.1:p.Thr769Ser
XM_005245088.1:c.2242A>T	XP_005245145.1:p.Thr748Ser
XM_005245088.2:c.2242A>T	XP_005245145.1:p.Thr748Ser
XM_017001035.1:c.2350A>T	XP_016856524.1:p.Thr784Ser