Canonical Allele Identifier: CA367241637

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438020G>T (hg19) ; chr7:g.29398404G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398404G>T , CM000669.2:g.29398404G>T	GRCh38
NC_000007.13:g.29438020G>T , CM000669.1:g.29438020G>T	GRCh37
NC_000007.12:g.29404545G>T	NCBI36
NG_029365.2:g.256858G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409350.6:c.247G>T	ENSP00000386968.2:p.Asp83Tyr
ENST00000439384.6:n.470G>T
ENST00000446446.6:c.208G>T	ENSP00000396867.2:p.Asp70Tyr
ENST00000706158.1:c.*152G>T	ENSP00000516236.1:n.*152G>T
ENST00000706159.1:c.120G>T	ENSP00000516237.1:p.Arg40=
ENST00000706160.1:c.208G>T	ENSP00000516238.1:p.Asp70Tyr
ENST00000706161.1:c.286G>T	ENSP00000516239.1:p.Asp96Tyr
ENST00000706162.1:c.208G>T	ENSP00000516240.1:p.Asp70Tyr
ENST00000706163.1:c.50-81875G>T	ENSP00000516241.1:n.50-81875G>T
ENST00000222792.11:c.208G>T MANE Select	ENSP00000222792.7:p.Asp70Tyr
ENST00000644824.1:c.433G>T	ENSP00000495614.1:p.Asp145Tyr
ENST00000222792.10:c.208G>T	ENSP00000222792.6:p.Asp70Tyr
ENST00000409350.5:c.247G>T	ENSP00000386968.1:p.Asp83Tyr
ENST00000409922.5:n.419G>T
ENST00000409964.6:n.407G>T
ENST00000412536.5:n.228G>T
ENST00000435288.6:c.168+4702G>T	ENSP00000400282.3:n.168+4702G>T
ENST00000439384.5:c.433G>T	ENSP00000409843.1:p.Asp145Tyr
ENST00000474070.5:c.308G>T
ENST00000478128.6:n.302G>T
ENST00000482820.6:n.417G>T
ENST00000491856.1:n.1757G>T
ENST00000495789.6:c.208G>T	ENSP00000438587.2:p.Asp70Tyr
ENST00000539389.5:c.208G>T	ENSP00000440526.2:p.Asp70Tyr
ENST00000539406.5:c.208G>T	ENSP00000444063.2:p.Asp70Tyr
NM_001293069.1:c.433G>T	NP_001279998.1:p.Asp145Tyr
NM_001293070.1:c.247G>T	NP_001279999.1:p.Asp83Tyr
NM_001293071.1:c.103G>T	NP_001280000.1:p.Asp35Tyr
NM_001293072.1:c.163G>T	NP_001280001.1:p.Asp55Tyr
NM_004067.3:c.208G>T	NP_004058.1:p.Asp70Tyr
XM_011515105.1:c.511G>T	XP_011513407.1:p.Asp171Tyr
XM_011515106.1:c.472G>T	XP_011513408.1:p.Asp158Tyr
XM_011515107.1:c.286G>T	XP_011513409.1:p.Asp96Tyr
XM_011515108.1:c.208G>T	XP_011513410.1:p.Asp70Tyr
XM_011515109.1:c.169G>T	XP_011513411.1:p.Asp57Tyr
XM_011515110.1:c.130G>T	XP_011513412.1:p.Asp44Tyr
XM_011515111.1:c.103G>T	XP_011513413.1:p.Asp35Tyr
XM_011515112.1:c.511G>T	XP_011513414.1:p.Asp171Tyr
XM_011515105.2:c.511G>T	XP_011513407.1:p.Asp171Tyr
XM_011515106.2:c.472G>T	XP_011513408.1:p.Asp158Tyr
XM_011515107.2:c.286G>T	XP_011513409.1:p.Asp96Tyr
XM_017011721.1:c.529G>T	XP_016867210.1:p.Asp177Tyr
XM_017011722.1:c.304G>T	XP_016867211.1:p.Asp102Tyr
NM_004067.4:c.208G>T MANE Select	NP_004058.1:p.Asp70Tyr
NM_001293070.2:c.247G>T	NP_001279999.1:p.Asp83Tyr
NM_001293071.2:c.103G>T	NP_001280000.1:p.Asp35Tyr
NM_001293072.2:c.163G>T	NP_001280001.1:p.Asp55Tyr
NM_001398427.1:c.-231G>T	NP_001385356.1:n.-231G>T