Canonical Allele Identifier: CA454421612

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438067C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398451C>T , CM000669.2:g.29398451C>T	GRCh38
NC_000007.13:g.29438067C>T , CM000669.1:g.29438067C>T	GRCh37
NC_000007.12:g.29404592C>T	NCBI36
NG_029365.2:g.256905C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.294C>T	ENSP00000386968.2:p.Ser98=
ENST00000439384.6:n.517C>T
ENST00000446446.6:c.255C>T	ENSP00000396867.2:p.Ser85=
ENST00000706158.1:c.*199C>T	ENSP00000516236.1:n.*199C>T
ENST00000706159.1:c.167C>T	ENSP00000516237.1:p.Ala56Val
ENST00000706160.1:c.255C>T	ENSP00000516238.1:p.Ser85=
ENST00000706161.1:c.333C>T	ENSP00000516239.1:p.Ser111=
ENST00000706162.1:c.255C>T	ENSP00000516240.1:p.Ser85=
ENST00000706163.1:c.50-81828C>T	ENSP00000516241.1:n.50-81828C>T
ENST00000222792.11:c.255C>T MANE Select	ENSP00000222792.7:p.Ser85=
ENST00000644824.1:c.480C>T	ENSP00000495614.1:p.Ser160=
ENST00000222792.10:c.255C>T	ENSP00000222792.6:p.Ser85=
ENST00000409350.5:c.294C>T	ENSP00000386968.1:p.Ser98=
ENST00000409922.5:n.466C>T
ENST00000409964.6:n.454C>T
ENST00000412536.5:n.275C>T
ENST00000435288.6:c.168+4749C>T	ENSP00000400282.3:n.168+4749C>T
ENST00000439384.5:c.480C>T	ENSP00000409843.1:p.Ser160=
ENST00000474070.5:c.355C>T
ENST00000478128.6:n.349C>T
ENST00000482820.6:n.464C>T
ENST00000491856.1:n.1804C>T
ENST00000495789.6:c.255C>T	ENSP00000438587.2:p.Ser85=
ENST00000539389.5:c.255C>T	ENSP00000440526.2:p.Ser85=
ENST00000539406.5:c.255C>T	ENSP00000444063.2:p.Ser85=
NM_001293069.1:c.480C>T	NP_001279998.1:p.Ser160=
NM_001293070.1:c.294C>T	NP_001279999.1:p.Ser98=
NM_001293071.1:c.150C>T	NP_001280000.1:p.Ser50=
NM_001293072.1:c.210C>T	NP_001280001.1:p.Ser70=
NM_004067.3:c.255C>T	NP_004058.1:p.Ser85=
XM_011515105.1:c.558C>T	XP_011513407.1:p.Ser186=
XM_011515106.1:c.519C>T	XP_011513408.1:p.Ser173=
XM_011515107.1:c.333C>T	XP_011513409.1:p.Ser111=
XM_011515108.1:c.255C>T	XP_011513410.1:p.Ser85=
XM_011515109.1:c.216C>T	XP_011513411.1:p.Ser72=
XM_011515110.1:c.177C>T	XP_011513412.1:p.Ser59=
XM_011515111.1:c.150C>T	XP_011513413.1:p.Ser50=
XM_011515112.1:c.558C>T	XP_011513414.1:p.Ser186=
XM_011515105.2:c.558C>T	XP_011513407.1:p.Ser186=
XM_011515106.2:c.519C>T	XP_011513408.1:p.Ser173=
XM_011515107.2:c.333C>T	XP_011513409.1:p.Ser111=
XM_017011721.1:c.576C>T	XP_016867210.1:p.Ser192=
XM_017011722.1:c.351C>T	XP_016867211.1:p.Ser117=
NM_004067.4:c.255C>T MANE Select	NP_004058.1:p.Ser85=
NM_001293070.2:c.294C>T	NP_001279999.1:p.Ser98=
NM_001293071.2:c.150C>T	NP_001280000.1:p.Ser50=
NM_001293072.2:c.210C>T	NP_001280001.1:p.Ser70=
NM_001398427.1:c.-184C>T	NP_001385356.1:n.-184C>T