Canonical Allele Identifier: CA1697231338

Gene: CHN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398475G= , CM000669.2:g.29398475G=	GRCh38
NC_000007.13:g.29438091G= , CM000669.1:g.29438091G=	GRCh37
NC_000007.12:g.29404616G=	NCBI36
NG_029365.2:g.256929G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.318G=	ENSP00000386968.2:p.Thr106=
ENST00000439384.6:n.541G=
ENST00000446446.6:c.279G=	ENSP00000396867.2:p.Thr93=
ENST00000706158.1:c.*223G=	ENSP00000516236.1:n.*223G=
ENST00000706159.1:c.191G=	ENSP00000516237.1:p.Arg64=
ENST00000706160.1:c.279G=	ENSP00000516238.1:p.Thr93=
ENST00000706161.1:c.357G=	ENSP00000516239.1:p.Thr119=
ENST00000706162.1:c.279G=	ENSP00000516240.1:p.Thr93=
ENST00000706163.1:c.50-81804G=	ENSP00000516241.1:n.50-81804G=
ENST00000222792.11:c.279G= MANE Select	ENSP00000222792.7:p.Thr93=
ENST00000644824.1:c.504G=	ENSP00000495614.1:p.Thr168=
ENST00000222792.10:c.279G=	ENSP00000222792.6:p.Thr93=
ENST00000409350.5:c.318G=	ENSP00000386968.1:p.Thr106=
ENST00000409922.5:n.490G=
ENST00000409964.6:n.478G=
ENST00000412536.5:n.299G=
ENST00000435288.6:c.168+4773G=	ENSP00000400282.3:n.168+4773G=
ENST00000439384.5:c.504G=	ENSP00000409843.1:p.Thr168=
ENST00000474070.5:c.379G=
ENST00000478128.6:n.373G=
ENST00000482820.6:n.488G=
ENST00000491856.1:n.1828G=
ENST00000495789.6:c.279G=	ENSP00000438587.2:p.Thr93=
ENST00000539389.5:c.279G=	ENSP00000440526.2:p.Thr93=
ENST00000539406.5:c.279G=	ENSP00000444063.2:p.Thr93=
NM_001293069.1:c.504G=	NP_001279998.1:p.Thr168=
NM_001293070.1:c.318G=	NP_001279999.1:p.Thr106=
NM_001293071.1:c.174G=	NP_001280000.1:p.Thr58=
NM_001293072.1:c.234G=	NP_001280001.1:p.Thr78=
NM_004067.3:c.279G=	NP_004058.1:p.Thr93=
XM_011515105.1:c.582G=	XP_011513407.1:p.Thr194=
XM_011515106.1:c.543G=	XP_011513408.1:p.Thr181=
XM_011515107.1:c.357G=	XP_011513409.1:p.Thr119=
XM_011515108.1:c.279G=	XP_011513410.1:p.Thr93=
XM_011515109.1:c.240G=	XP_011513411.1:p.Thr80=
XM_011515110.1:c.201G=	XP_011513412.1:p.Thr67=
XM_011515111.1:c.174G=	XP_011513413.1:p.Thr58=
XM_011515112.1:c.582G=	XP_011513414.1:p.Thr194=
XM_011515105.2:c.582G=	XP_011513407.1:p.Thr194=
XM_011515106.2:c.543G=	XP_011513408.1:p.Thr181=
XM_011515107.2:c.357G=	XP_011513409.1:p.Thr119=
XM_017011721.1:c.600G=	XP_016867210.1:p.Thr200=
XM_017011722.1:c.375G=	XP_016867211.1:p.Thr125=
NM_004067.4:c.279G= MANE Select	NP_004058.1:p.Thr93=
NM_001293070.2:c.318G=	NP_001279999.1:p.Thr106=
NM_001293071.2:c.174G=	NP_001280000.1:p.Thr58=
NM_001293072.2:c.234G=	NP_001280001.1:p.Thr78=
NM_001398427.1:c.-160G=	NP_001385356.1:n.-160G=