Canonical Allele Identifier: CA367241640

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438021A>T (hg19) ; chr7:g.29398405A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398405A>T , CM000669.2:g.29398405A>T	GRCh38
NC_000007.13:g.29438021A>T , CM000669.1:g.29438021A>T	GRCh37
NC_000007.12:g.29404546A>T	NCBI36
NG_029365.2:g.256859A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409350.6:c.248A>T	ENSP00000386968.2:p.Asp83Val
ENST00000439384.6:n.471A>T
ENST00000446446.6:c.209A>T	ENSP00000396867.2:p.Asp70Val
ENST00000706158.1:c.*153A>T	ENSP00000516236.1:n.*153A>T
ENST00000706159.1:c.121A>T	ENSP00000516237.1:p.Met41Leu
ENST00000706160.1:c.209A>T	ENSP00000516238.1:p.Asp70Val
ENST00000706161.1:c.287A>T	ENSP00000516239.1:p.Asp96Val
ENST00000706162.1:c.209A>T	ENSP00000516240.1:p.Asp70Val
ENST00000706163.1:c.50-81874A>T	ENSP00000516241.1:n.50-81874A>T
ENST00000222792.11:c.209A>T MANE Select	ENSP00000222792.7:p.Asp70Val
ENST00000644824.1:c.434A>T	ENSP00000495614.1:p.Asp145Val
ENST00000222792.10:c.209A>T	ENSP00000222792.6:p.Asp70Val
ENST00000409350.5:c.248A>T	ENSP00000386968.1:p.Asp83Val
ENST00000409922.5:n.420A>T
ENST00000409964.6:n.408A>T
ENST00000412536.5:n.229A>T
ENST00000435288.6:c.168+4703A>T	ENSP00000400282.3:n.168+4703A>T
ENST00000439384.5:c.434A>T	ENSP00000409843.1:p.Asp145Val
ENST00000474070.5:c.309A>T
ENST00000478128.6:n.303A>T
ENST00000482820.6:n.418A>T
ENST00000491856.1:n.1758A>T
ENST00000495789.6:c.209A>T	ENSP00000438587.2:p.Asp70Val
ENST00000539389.5:c.209A>T	ENSP00000440526.2:p.Asp70Val
ENST00000539406.5:c.209A>T	ENSP00000444063.2:p.Asp70Val
NM_001293069.1:c.434A>T	NP_001279998.1:p.Asp145Val
NM_001293070.1:c.248A>T	NP_001279999.1:p.Asp83Val
NM_001293071.1:c.104A>T	NP_001280000.1:p.Asp35Val
NM_001293072.1:c.164A>T	NP_001280001.1:p.Asp55Val
NM_004067.3:c.209A>T	NP_004058.1:p.Asp70Val
XM_011515105.1:c.512A>T	XP_011513407.1:p.Asp171Val
XM_011515106.1:c.473A>T	XP_011513408.1:p.Asp158Val
XM_011515107.1:c.287A>T	XP_011513409.1:p.Asp96Val
XM_011515108.1:c.209A>T	XP_011513410.1:p.Asp70Val
XM_011515109.1:c.170A>T	XP_011513411.1:p.Asp57Val
XM_011515110.1:c.131A>T	XP_011513412.1:p.Asp44Val
XM_011515111.1:c.104A>T	XP_011513413.1:p.Asp35Val
XM_011515112.1:c.512A>T	XP_011513414.1:p.Asp171Val
XM_011515105.2:c.512A>T	XP_011513407.1:p.Asp171Val
XM_011515106.2:c.473A>T	XP_011513408.1:p.Asp158Val
XM_011515107.2:c.287A>T	XP_011513409.1:p.Asp96Val
XM_017011721.1:c.530A>T	XP_016867210.1:p.Asp177Val
XM_017011722.1:c.305A>T	XP_016867211.1:p.Asp102Val
NM_004067.4:c.209A>T MANE Select	NP_004058.1:p.Asp70Val
NM_001293070.2:c.248A>T	NP_001279999.1:p.Asp83Val
NM_001293071.2:c.104A>T	NP_001280000.1:p.Asp35Val
NM_001293072.2:c.164A>T	NP_001280001.1:p.Asp55Val
NM_001398427.1:c.-230A>T	NP_001385356.1:n.-230A>T