Canonical Allele Identifier: CA367241693

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438048C>A (hg19) ; chr7:g.29398432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398432C>A , CM000669.2:g.29398432C>A	GRCh38
NC_000007.13:g.29438048C>A , CM000669.1:g.29438048C>A	GRCh37
NC_000007.12:g.29404573C>A	NCBI36
NG_029365.2:g.256886C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.275C>A	ENSP00000386968.2:p.Ala92Asp
ENST00000439384.6:n.498C>A
ENST00000446446.6:c.236C>A	ENSP00000396867.2:p.Ala79Asp
ENST00000706158.1:c.*180C>A	ENSP00000516236.1:n.*180C>A
ENST00000706159.1:c.148C>A	ENSP00000516237.1:p.Pro50Thr
ENST00000706160.1:c.236C>A	ENSP00000516238.1:p.Ala79Asp
ENST00000706161.1:c.314C>A	ENSP00000516239.1:p.Ala105Asp
ENST00000706162.1:c.236C>A	ENSP00000516240.1:p.Ala79Asp
ENST00000706163.1:c.50-81847C>A	ENSP00000516241.1:n.50-81847C>A
ENST00000222792.11:c.236C>A MANE Select	ENSP00000222792.7:p.Ala79Asp
ENST00000644824.1:c.461C>A	ENSP00000495614.1:p.Ala154Asp
ENST00000222792.10:c.236C>A	ENSP00000222792.6:p.Ala79Asp
ENST00000409350.5:c.275C>A	ENSP00000386968.1:p.Ala92Asp
ENST00000409922.5:n.447C>A
ENST00000409964.6:n.435C>A
ENST00000412536.5:n.256C>A
ENST00000435288.6:c.168+4730C>A	ENSP00000400282.3:n.168+4730C>A
ENST00000439384.5:c.461C>A	ENSP00000409843.1:p.Ala154Asp
ENST00000474070.5:c.336C>A
ENST00000478128.6:n.330C>A
ENST00000482820.6:n.445C>A
ENST00000491856.1:n.1785C>A
ENST00000495789.6:c.236C>A	ENSP00000438587.2:p.Ala79Asp
ENST00000539389.5:c.236C>A	ENSP00000440526.2:p.Ala79Asp
ENST00000539406.5:c.236C>A	ENSP00000444063.2:p.Ala79Asp
NM_001293069.1:c.461C>A	NP_001279998.1:p.Ala154Asp
NM_001293070.1:c.275C>A	NP_001279999.1:p.Ala92Asp
NM_001293071.1:c.131C>A	NP_001280000.1:p.Ala44Asp
NM_001293072.1:c.191C>A	NP_001280001.1:p.Ala64Asp
NM_004067.3:c.236C>A	NP_004058.1:p.Ala79Asp
XM_011515105.1:c.539C>A	XP_011513407.1:p.Ala180Asp
XM_011515106.1:c.500C>A	XP_011513408.1:p.Ala167Asp
XM_011515107.1:c.314C>A	XP_011513409.1:p.Ala105Asp
XM_011515108.1:c.236C>A	XP_011513410.1:p.Ala79Asp
XM_011515109.1:c.197C>A	XP_011513411.1:p.Ala66Asp
XM_011515110.1:c.158C>A	XP_011513412.1:p.Ala53Asp
XM_011515111.1:c.131C>A	XP_011513413.1:p.Ala44Asp
XM_011515112.1:c.539C>A	XP_011513414.1:p.Ala180Asp
XM_011515105.2:c.539C>A	XP_011513407.1:p.Ala180Asp
XM_011515106.2:c.500C>A	XP_011513408.1:p.Ala167Asp
XM_011515107.2:c.314C>A	XP_011513409.1:p.Ala105Asp
XM_017011721.1:c.557C>A	XP_016867210.1:p.Ala186Asp
XM_017011722.1:c.332C>A	XP_016867211.1:p.Ala111Asp
NM_004067.4:c.236C>A MANE Select	NP_004058.1:p.Ala79Asp
NM_001293070.2:c.275C>A	NP_001279999.1:p.Ala92Asp
NM_001293071.2:c.131C>A	NP_001280000.1:p.Ala44Asp
NM_001293072.2:c.191C>A	NP_001280001.1:p.Ala64Asp
NM_001398427.1:c.-203C>A	NP_001385356.1:n.-203C>A