Canonical Allele Identifier: CA454421625

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438085C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398469C>T , CM000669.2:g.29398469C>T	GRCh38
NC_000007.13:g.29438085C>T , CM000669.1:g.29438085C>T	GRCh37
NC_000007.12:g.29404610C>T	NCBI36
NG_029365.2:g.256923C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.312C>T	ENSP00000386968.2:p.Cys104=
ENST00000439384.6:n.535C>T
ENST00000446446.6:c.273C>T	ENSP00000396867.2:p.Cys91=
ENST00000706158.1:c.*217C>T	ENSP00000516236.1:n.*217C>T
ENST00000706159.1:c.185C>T	ENSP00000516237.1:p.Ala62Val
ENST00000706160.1:c.273C>T	ENSP00000516238.1:p.Cys91=
ENST00000706161.1:c.351C>T	ENSP00000516239.1:p.Cys117=
ENST00000706162.1:c.273C>T	ENSP00000516240.1:p.Cys91=
ENST00000706163.1:c.50-81810C>T	ENSP00000516241.1:n.50-81810C>T
ENST00000222792.11:c.273C>T MANE Select	ENSP00000222792.7:p.Cys91=
ENST00000644824.1:c.498C>T	ENSP00000495614.1:p.Cys166=
ENST00000222792.10:c.273C>T	ENSP00000222792.6:p.Cys91=
ENST00000409350.5:c.312C>T	ENSP00000386968.1:p.Cys104=
ENST00000409922.5:n.484C>T
ENST00000409964.6:n.472C>T
ENST00000412536.5:n.293C>T
ENST00000435288.6:c.168+4767C>T	ENSP00000400282.3:n.168+4767C>T
ENST00000439384.5:c.498C>T	ENSP00000409843.1:p.Cys166=
ENST00000474070.5:c.373C>T
ENST00000478128.6:n.367C>T
ENST00000482820.6:n.482C>T
ENST00000491856.1:n.1822C>T
ENST00000495789.6:c.273C>T	ENSP00000438587.2:p.Cys91=
ENST00000539389.5:c.273C>T	ENSP00000440526.2:p.Cys91=
ENST00000539406.5:c.273C>T	ENSP00000444063.2:p.Cys91=
NM_001293069.1:c.498C>T	NP_001279998.1:p.Cys166=
NM_001293070.1:c.312C>T	NP_001279999.1:p.Cys104=
NM_001293071.1:c.168C>T	NP_001280000.1:p.Cys56=
NM_001293072.1:c.228C>T	NP_001280001.1:p.Cys76=
NM_004067.3:c.273C>T	NP_004058.1:p.Cys91=
XM_011515105.1:c.576C>T	XP_011513407.1:p.Cys192=
XM_011515106.1:c.537C>T	XP_011513408.1:p.Cys179=
XM_011515107.1:c.351C>T	XP_011513409.1:p.Cys117=
XM_011515108.1:c.273C>T	XP_011513410.1:p.Cys91=
XM_011515109.1:c.234C>T	XP_011513411.1:p.Cys78=
XM_011515110.1:c.195C>T	XP_011513412.1:p.Cys65=
XM_011515111.1:c.168C>T	XP_011513413.1:p.Cys56=
XM_011515112.1:c.576C>T	XP_011513414.1:p.Cys192=
XM_011515105.2:c.576C>T	XP_011513407.1:p.Cys192=
XM_011515106.2:c.537C>T	XP_011513408.1:p.Cys179=
XM_011515107.2:c.351C>T	XP_011513409.1:p.Cys117=
XM_017011721.1:c.594C>T	XP_016867210.1:p.Cys198=
XM_017011722.1:c.369C>T	XP_016867211.1:p.Cys123=
NM_004067.4:c.273C>T MANE Select	NP_004058.1:p.Cys91=
NM_001293070.2:c.312C>T	NP_001279999.1:p.Cys104=
NM_001293071.2:c.168C>T	NP_001280000.1:p.Cys56=
NM_001293072.2:c.228C>T	NP_001280001.1:p.Cys76=
NM_001398427.1:c.-166C>T	NP_001385356.1:n.-166C>T