Canonical Allele Identifier: CA367241726

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438062G>T (hg19) ; chr7:g.29398446G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398446G>T , CM000669.2:g.29398446G>T	GRCh38
NC_000007.13:g.29438062G>T , CM000669.1:g.29438062G>T	GRCh37
NC_000007.12:g.29404587G>T	NCBI36
NG_029365.2:g.256900G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.289G>T	ENSP00000386968.2:p.Glu97Ter
ENST00000439384.6:n.512G>T
ENST00000446446.6:c.250G>T	ENSP00000396867.2:p.Glu84Ter
ENST00000706158.1:c.*194G>T	ENSP00000516236.1:n.*194G>T
ENST00000706159.1:c.162G>T	ENSP00000516237.1:p.Glu54Asp
ENST00000706160.1:c.250G>T	ENSP00000516238.1:p.Glu84Ter
ENST00000706161.1:c.328G>T	ENSP00000516239.1:p.Glu110Ter
ENST00000706162.1:c.250G>T	ENSP00000516240.1:p.Glu84Ter
ENST00000706163.1:c.50-81833G>T	ENSP00000516241.1:n.50-81833G>T
ENST00000222792.11:c.250G>T MANE Select	ENSP00000222792.7:p.Glu84Ter
ENST00000644824.1:c.475G>T	ENSP00000495614.1:p.Glu159Ter
ENST00000222792.10:c.250G>T	ENSP00000222792.6:p.Glu84Ter
ENST00000409350.5:c.289G>T	ENSP00000386968.1:p.Glu97Ter
ENST00000409922.5:n.461G>T
ENST00000409964.6:n.449G>T
ENST00000412536.5:n.270G>T
ENST00000435288.6:c.168+4744G>T	ENSP00000400282.3:n.168+4744G>T
ENST00000439384.5:c.475G>T	ENSP00000409843.1:p.Glu159Ter
ENST00000474070.5:c.350G>T
ENST00000478128.6:n.344G>T
ENST00000482820.6:n.459G>T
ENST00000491856.1:n.1799G>T
ENST00000495789.6:c.250G>T	ENSP00000438587.2:p.Glu84Ter
ENST00000539389.5:c.250G>T	ENSP00000440526.2:p.Glu84Ter
ENST00000539406.5:c.250G>T	ENSP00000444063.2:p.Glu84Ter
NM_001293069.1:c.475G>T	NP_001279998.1:p.Glu159Ter
NM_001293070.1:c.289G>T	NP_001279999.1:p.Glu97Ter
NM_001293071.1:c.145G>T	NP_001280000.1:p.Glu49Ter
NM_001293072.1:c.205G>T	NP_001280001.1:p.Glu69Ter
NM_004067.3:c.250G>T	NP_004058.1:p.Glu84Ter
XM_011515105.1:c.553G>T	XP_011513407.1:p.Glu185Ter
XM_011515106.1:c.514G>T	XP_011513408.1:p.Glu172Ter
XM_011515107.1:c.328G>T	XP_011513409.1:p.Glu110Ter
XM_011515108.1:c.250G>T	XP_011513410.1:p.Glu84Ter
XM_011515109.1:c.211G>T	XP_011513411.1:p.Glu71Ter
XM_011515110.1:c.172G>T	XP_011513412.1:p.Glu58Ter
XM_011515111.1:c.145G>T	XP_011513413.1:p.Glu49Ter
XM_011515112.1:c.553G>T	XP_011513414.1:p.Glu185Ter
XM_011515105.2:c.553G>T	XP_011513407.1:p.Glu185Ter
XM_011515106.2:c.514G>T	XP_011513408.1:p.Glu172Ter
XM_011515107.2:c.328G>T	XP_011513409.1:p.Glu110Ter
XM_017011721.1:c.571G>T	XP_016867210.1:p.Glu191Ter
XM_017011722.1:c.346G>T	XP_016867211.1:p.Glu116Ter
NM_004067.4:c.250G>T MANE Select	NP_004058.1:p.Glu84Ter
NM_001293070.2:c.289G>T	NP_001279999.1:p.Glu97Ter
NM_001293071.2:c.145G>T	NP_001280000.1:p.Glu49Ter
NM_001293072.2:c.205G>T	NP_001280001.1:p.Glu69Ter
NM_001398427.1:c.-189G>T	NP_001385356.1:n.-189G>T