Canonical Allele Identifier: CA1697226937

Gene: CHN2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29388497C= , CM000669.2:g.29388497C=	GRCh38
NC_000007.13:g.29428113C= , CM000669.1:g.29428113C=	GRCh37
NC_000007.12:g.29394638C=	NCBI36
NG_029365.2:g.246951C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.184-5182C=	ENSP00000386968.2:n.184-5182C=
ENST00000439384.6:n.407-5182C=
ENST00000446446.6:c.145-5182C=	ENSP00000396867.2:n.145-5182C=
ENST00000706158.1:c.*89-5182C=	ENSP00000516236.1:n.*89-5182C=
ENST00000706159.1:c.89-9876C=	ENSP00000516237.1:n.89-9876C=
ENST00000706160.1:c.145-5182C=	ENSP00000516238.1:n.145-5182C=
ENST00000706161.1:c.223-5182C=	ENSP00000516239.1:n.223-5182C=
ENST00000706162.1:c.145-5182C=	ENSP00000516240.1:n.145-5182C=
ENST00000706163.1:c.50-91782C=	ENSP00000516241.1:n.50-91782C=
ENST00000222792.11:c.145-5182C= MANE Select	ENSP00000222792.7:n.145-5182C=
ENST00000644824.1:c.370-5182C=	ENSP00000495614.1:n.370-5182C=
ENST00000222792.10:c.145-5182C=	ENSP00000222792.6:n.145-5182C=
ENST00000409350.5:c.184-5182C=	ENSP00000386968.1:n.184-5182C=
ENST00000409922.5:n.356-5182C=
ENST00000409964.6:n.344-5182C=
ENST00000412536.5:n.165-5182C=
ENST00000435288.6:c.145-5182C=	ENSP00000400282.3:n.145-5182C=
ENST00000439384.5:c.370-5182C=	ENSP00000409843.1:n.370-5182C=
ENST00000474070.5:c.245-5182C=
ENST00000478128.6:n.239-5182C=
ENST00000482820.6:n.354-5182C=
ENST00000495789.6:c.145-5182C=	ENSP00000438587.2:n.145-5182C=
ENST00000539389.5:c.145-5182C=	ENSP00000440526.2:n.145-5182C=
ENST00000539406.5:c.145-5182C=	ENSP00000444063.2:n.145-5182C=
NM_001293069.1:c.370-5182C=	NP_001279998.1:n.370-5182C=
NM_001293070.1:c.184-5182C=	NP_001279999.1:n.184-5182C=
NM_001293071.1:c.40-5182C=	NP_001280000.1:n.40-5182C=
NM_001293072.1:c.100-5182C=	NP_001280001.1:n.100-5182C=
NM_004067.3:c.145-5182C=	NP_004058.1:n.145-5182C=
XM_011515105.1:c.448-5182C=	XP_011513407.1:n.448-5182C=
XM_011515106.1:c.409-5182C=	XP_011513408.1:n.409-5182C=
XM_011515107.1:c.223-5182C=	XP_011513409.1:n.223-5182C=
XM_011515108.1:c.145-5182C=	XP_011513410.1:n.145-5182C=
XM_011515109.1:c.106-5182C=	XP_011513411.1:n.106-5182C=
XM_011515110.1:c.67-5182C=	XP_011513412.1:n.67-5182C=
XM_011515111.1:c.40-5182C=	XP_011513413.1:n.40-5182C=
XM_011515112.1:c.448-5182C=	XP_011513414.1:n.448-5182C=
XM_011515105.2:c.448-5182C=	XP_011513407.1:n.448-5182C=
XM_011515106.2:c.409-5182C=	XP_011513408.1:n.409-5182C=
XM_011515107.2:c.223-5182C=	XP_011513409.1:n.223-5182C=
XM_017011721.1:c.466-5182C=	XP_016867210.1:n.466-5182C=
XM_017011722.1:c.241-5182C=	XP_016867211.1:n.241-5182C=
NM_004067.4:c.145-5182C= MANE Select	NP_004058.1:n.145-5182C=
NM_001293070.2:c.184-5182C=	NP_001279999.1:n.184-5182C=
NM_001293071.2:c.40-5182C=	NP_001280000.1:n.40-5182C=
NM_001293072.2:c.100-5182C=	NP_001280001.1:n.100-5182C=
NM_001398427.1:c.-294-5182C=	NP_001385356.1:n.-294-5182C=