Canonical Allele Identifier: CA367241702

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438052C>A (hg19) ; chr7:g.29398436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398436C>A , CM000669.2:g.29398436C>A	GRCh38
NC_000007.13:g.29438052C>A , CM000669.1:g.29438052C>A	GRCh37
NC_000007.12:g.29404577C>A	NCBI36
NG_029365.2:g.256890C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.279C>A	ENSP00000386968.2:p.Tyr93Ter
ENST00000439384.6:n.502C>A
ENST00000446446.6:c.240C>A	ENSP00000396867.2:p.Tyr80Ter
ENST00000706158.1:c.*184C>A	ENSP00000516236.1:n.*184C>A
ENST00000706159.1:c.152C>A	ENSP00000516237.1:p.Thr51Lys
ENST00000706160.1:c.240C>A	ENSP00000516238.1:p.Tyr80Ter
ENST00000706161.1:c.318C>A	ENSP00000516239.1:p.Tyr106Ter
ENST00000706162.1:c.240C>A	ENSP00000516240.1:p.Tyr80Ter
ENST00000706163.1:c.50-81843C>A	ENSP00000516241.1:n.50-81843C>A
ENST00000222792.11:c.240C>A MANE Select	ENSP00000222792.7:p.Tyr80Ter
ENST00000644824.1:c.465C>A	ENSP00000495614.1:p.Tyr155Ter
ENST00000222792.10:c.240C>A	ENSP00000222792.6:p.Tyr80Ter
ENST00000409350.5:c.279C>A	ENSP00000386968.1:p.Tyr93Ter
ENST00000409922.5:n.451C>A
ENST00000409964.6:n.439C>A
ENST00000412536.5:n.260C>A
ENST00000435288.6:c.168+4734C>A	ENSP00000400282.3:n.168+4734C>A
ENST00000439384.5:c.465C>A	ENSP00000409843.1:p.Tyr155Ter
ENST00000474070.5:c.340C>A
ENST00000478128.6:n.334C>A
ENST00000482820.6:n.449C>A
ENST00000491856.1:n.1789C>A
ENST00000495789.6:c.240C>A	ENSP00000438587.2:p.Tyr80Ter
ENST00000539389.5:c.240C>A	ENSP00000440526.2:p.Tyr80Ter
ENST00000539406.5:c.240C>A	ENSP00000444063.2:p.Tyr80Ter
NM_001293069.1:c.465C>A	NP_001279998.1:p.Tyr155Ter
NM_001293070.1:c.279C>A	NP_001279999.1:p.Tyr93Ter
NM_001293071.1:c.135C>A	NP_001280000.1:p.Tyr45Ter
NM_001293072.1:c.195C>A	NP_001280001.1:p.Tyr65Ter
NM_004067.3:c.240C>A	NP_004058.1:p.Tyr80Ter
XM_011515105.1:c.543C>A	XP_011513407.1:p.Tyr181Ter
XM_011515106.1:c.504C>A	XP_011513408.1:p.Tyr168Ter
XM_011515107.1:c.318C>A	XP_011513409.1:p.Tyr106Ter
XM_011515108.1:c.240C>A	XP_011513410.1:p.Tyr80Ter
XM_011515109.1:c.201C>A	XP_011513411.1:p.Tyr67Ter
XM_011515110.1:c.162C>A	XP_011513412.1:p.Tyr54Ter
XM_011515111.1:c.135C>A	XP_011513413.1:p.Tyr45Ter
XM_011515112.1:c.543C>A	XP_011513414.1:p.Tyr181Ter
XM_011515105.2:c.543C>A	XP_011513407.1:p.Tyr181Ter
XM_011515106.2:c.504C>A	XP_011513408.1:p.Tyr168Ter
XM_011515107.2:c.318C>A	XP_011513409.1:p.Tyr106Ter
XM_017011721.1:c.561C>A	XP_016867210.1:p.Tyr187Ter
XM_017011722.1:c.336C>A	XP_016867211.1:p.Tyr112Ter
NM_004067.4:c.240C>A MANE Select	NP_004058.1:p.Tyr80Ter
NM_001293070.2:c.279C>A	NP_001279999.1:p.Tyr93Ter
NM_001293071.2:c.135C>A	NP_001280000.1:p.Tyr45Ter
NM_001293072.2:c.195C>A	NP_001280001.1:p.Tyr65Ter
NM_001398427.1:c.-199C>A	NP_001385356.1:n.-199C>A