Canonical Allele Identifier: CA367241620

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438012A>T (hg19) ; chr7:g.29398396A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398396A>T , CM000669.2:g.29398396A>T	GRCh38
NC_000007.13:g.29438012A>T , CM000669.1:g.29438012A>T	GRCh37
NC_000007.12:g.29404537A>T	NCBI36
NG_029365.2:g.256850A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.239A>T	ENSP00000386968.2:p.Glu80Val
ENST00000439384.6:n.462A>T
ENST00000446446.6:c.200A>T	ENSP00000396867.2:p.Glu67Val
ENST00000706158.1:c.*144A>T	ENSP00000516236.1:n.*144A>T
ENST00000706159.1:c.112A>T	ENSP00000516237.1:p.Ser38Cys
ENST00000706160.1:c.200A>T	ENSP00000516238.1:p.Glu67Val
ENST00000706161.1:c.278A>T	ENSP00000516239.1:p.Glu93Val
ENST00000706162.1:c.200A>T	ENSP00000516240.1:p.Glu67Val
ENST00000706163.1:c.50-81883A>T	ENSP00000516241.1:n.50-81883A>T
ENST00000222792.11:c.200A>T MANE Select	ENSP00000222792.7:p.Glu67Val
ENST00000644824.1:c.425A>T	ENSP00000495614.1:p.Glu142Val
ENST00000222792.10:c.200A>T	ENSP00000222792.6:p.Glu67Val
ENST00000409350.5:c.239A>T	ENSP00000386968.1:p.Glu80Val
ENST00000409922.5:n.411A>T
ENST00000409964.6:n.399A>T
ENST00000412536.5:n.220A>T
ENST00000435288.6:c.168+4694A>T	ENSP00000400282.3:n.168+4694A>T
ENST00000439384.5:c.425A>T	ENSP00000409843.1:p.Glu142Val
ENST00000474070.5:c.300A>T
ENST00000478128.6:n.294A>T
ENST00000482820.6:n.409A>T
ENST00000491856.1:n.1749A>T
ENST00000495789.6:c.200A>T	ENSP00000438587.2:p.Glu67Val
ENST00000539389.5:c.200A>T	ENSP00000440526.2:p.Glu67Val
ENST00000539406.5:c.200A>T	ENSP00000444063.2:p.Glu67Val
NM_001293069.1:c.425A>T	NP_001279998.1:p.Glu142Val
NM_001293070.1:c.239A>T	NP_001279999.1:p.Glu80Val
NM_001293071.1:c.95A>T	NP_001280000.1:p.Glu32Val
NM_001293072.1:c.155A>T	NP_001280001.1:p.Glu52Val
NM_004067.3:c.200A>T	NP_004058.1:p.Glu67Val
XM_011515105.1:c.503A>T	XP_011513407.1:p.Glu168Val
XM_011515106.1:c.464A>T	XP_011513408.1:p.Glu155Val
XM_011515107.1:c.278A>T	XP_011513409.1:p.Glu93Val
XM_011515108.1:c.200A>T	XP_011513410.1:p.Glu67Val
XM_011515109.1:c.161A>T	XP_011513411.1:p.Glu54Val
XM_011515110.1:c.122A>T	XP_011513412.1:p.Glu41Val
XM_011515111.1:c.95A>T	XP_011513413.1:p.Glu32Val
XM_011515112.1:c.503A>T	XP_011513414.1:p.Glu168Val
XM_011515105.2:c.503A>T	XP_011513407.1:p.Glu168Val
XM_011515106.2:c.464A>T	XP_011513408.1:p.Glu155Val
XM_011515107.2:c.278A>T	XP_011513409.1:p.Glu93Val
XM_017011721.1:c.521A>T	XP_016867210.1:p.Glu174Val
XM_017011722.1:c.296A>T	XP_016867211.1:p.Glu99Val
NM_004067.4:c.200A>T MANE Select	NP_004058.1:p.Glu67Val
NM_001293070.2:c.239A>T	NP_001279999.1:p.Glu80Val
NM_001293071.2:c.95A>T	NP_001280000.1:p.Glu32Val
NM_001293072.2:c.155A>T	NP_001280001.1:p.Glu52Val
NM_001398427.1:c.-239A>T	NP_001385356.1:n.-239A>T