Canonical Allele Identifier: CA1697231328

Gene: CHN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398437A= , CM000669.2:g.29398437A=	GRCh38
NC_000007.13:g.29438053A= , CM000669.1:g.29438053A=	GRCh37
NC_000007.12:g.29404578A=	NCBI36
NG_029365.2:g.256891A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.280A=	ENSP00000386968.2:p.Ile94=
ENST00000439384.6:n.503A=
ENST00000446446.6:c.241A=	ENSP00000396867.2:p.Ile81=
ENST00000706158.1:c.*185A=	ENSP00000516236.1:n.*185A=
ENST00000706159.1:c.153A=	ENSP00000516237.1:p.Thr51=
ENST00000706160.1:c.241A=	ENSP00000516238.1:p.Ile81=
ENST00000706161.1:c.319A=	ENSP00000516239.1:p.Ile107=
ENST00000706162.1:c.241A=	ENSP00000516240.1:p.Ile81=
ENST00000706163.1:c.50-81842A=	ENSP00000516241.1:n.50-81842A=
ENST00000222792.11:c.241A= MANE Select	ENSP00000222792.7:p.Ile81=
ENST00000644824.1:c.466A=	ENSP00000495614.1:p.Ile156=
ENST00000222792.10:c.241A=	ENSP00000222792.6:p.Ile81=
ENST00000409350.5:c.280A=	ENSP00000386968.1:p.Ile94=
ENST00000409922.5:n.452A=
ENST00000409964.6:n.440A=
ENST00000412536.5:n.261A=
ENST00000435288.6:c.168+4735A=	ENSP00000400282.3:n.168+4735A=
ENST00000439384.5:c.466A=	ENSP00000409843.1:p.Ile156=
ENST00000474070.5:c.341A=
ENST00000478128.6:n.335A=
ENST00000482820.6:n.450A=
ENST00000491856.1:n.1790A=
ENST00000495789.6:c.241A=	ENSP00000438587.2:p.Ile81=
ENST00000539389.5:c.241A=	ENSP00000440526.2:p.Ile81=
ENST00000539406.5:c.241A=	ENSP00000444063.2:p.Ile81=
NM_001293069.1:c.466A=	NP_001279998.1:p.Ile156=
NM_001293070.1:c.280A=	NP_001279999.1:p.Ile94=
NM_001293071.1:c.136A=	NP_001280000.1:p.Ile46=
NM_001293072.1:c.196A=	NP_001280001.1:p.Ile66=
NM_004067.3:c.241A=	NP_004058.1:p.Ile81=
XM_011515105.1:c.544A=	XP_011513407.1:p.Ile182=
XM_011515106.1:c.505A=	XP_011513408.1:p.Ile169=
XM_011515107.1:c.319A=	XP_011513409.1:p.Ile107=
XM_011515108.1:c.241A=	XP_011513410.1:p.Ile81=
XM_011515109.1:c.202A=	XP_011513411.1:p.Ile68=
XM_011515110.1:c.163A=	XP_011513412.1:p.Ile55=
XM_011515111.1:c.136A=	XP_011513413.1:p.Ile46=
XM_011515112.1:c.544A=	XP_011513414.1:p.Ile182=
XM_011515105.2:c.544A=	XP_011513407.1:p.Ile182=
XM_011515106.2:c.505A=	XP_011513408.1:p.Ile169=
XM_011515107.2:c.319A=	XP_011513409.1:p.Ile107=
XM_017011721.1:c.562A=	XP_016867210.1:p.Ile188=
XM_017011722.1:c.337A=	XP_016867211.1:p.Ile113=
NM_004067.4:c.241A= MANE Select	NP_004058.1:p.Ile81=
NM_001293070.2:c.280A=	NP_001279999.1:p.Ile94=
NM_001293071.2:c.136A=	NP_001280000.1:p.Ile46=
NM_001293072.2:c.196A=	NP_001280001.1:p.Ile66=
NM_001398427.1:c.-198A=	NP_001385356.1:n.-198A=