Canonical Allele Identifier: CA367241621

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438013G>C (hg19) ; chr7:g.29398397G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398397G>C , CM000669.2:g.29398397G>C	GRCh38
NC_000007.13:g.29438013G>C , CM000669.1:g.29438013G>C	GRCh37
NC_000007.12:g.29404538G>C	NCBI36
NG_029365.2:g.256851G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409350.6:c.240G>C	ENSP00000386968.2:p.Glu80Asp
ENST00000439384.6:n.463G>C
ENST00000446446.6:c.201G>C	ENSP00000396867.2:p.Glu67Asp
ENST00000706158.1:c.*145G>C	ENSP00000516236.1:n.*145G>C
ENST00000706159.1:c.113G>C	ENSP00000516237.1:p.Ser38Thr
ENST00000706160.1:c.201G>C	ENSP00000516238.1:p.Glu67Asp
ENST00000706161.1:c.279G>C	ENSP00000516239.1:p.Glu93Asp
ENST00000706162.1:c.201G>C	ENSP00000516240.1:p.Glu67Asp
ENST00000706163.1:c.50-81882G>C	ENSP00000516241.1:n.50-81882G>C
ENST00000222792.11:c.201G>C MANE Select	ENSP00000222792.7:p.Glu67Asp
ENST00000644824.1:c.426G>C	ENSP00000495614.1:p.Glu142Asp
ENST00000222792.10:c.201G>C	ENSP00000222792.6:p.Glu67Asp
ENST00000409350.5:c.240G>C	ENSP00000386968.1:p.Glu80Asp
ENST00000409922.5:n.412G>C
ENST00000409964.6:n.400G>C
ENST00000412536.5:n.221G>C
ENST00000435288.6:c.168+4695G>C	ENSP00000400282.3:n.168+4695G>C
ENST00000439384.5:c.426G>C	ENSP00000409843.1:p.Glu142Asp
ENST00000474070.5:c.301G>C
ENST00000478128.6:n.295G>C
ENST00000482820.6:n.410G>C
ENST00000491856.1:n.1750G>C
ENST00000495789.6:c.201G>C	ENSP00000438587.2:p.Glu67Asp
ENST00000539389.5:c.201G>C	ENSP00000440526.2:p.Glu67Asp
ENST00000539406.5:c.201G>C	ENSP00000444063.2:p.Glu67Asp
NM_001293069.1:c.426G>C	NP_001279998.1:p.Glu142Asp
NM_001293070.1:c.240G>C	NP_001279999.1:p.Glu80Asp
NM_001293071.1:c.96G>C	NP_001280000.1:p.Glu32Asp
NM_001293072.1:c.156G>C	NP_001280001.1:p.Glu52Asp
NM_004067.3:c.201G>C	NP_004058.1:p.Glu67Asp
XM_011515105.1:c.504G>C	XP_011513407.1:p.Glu168Asp
XM_011515106.1:c.465G>C	XP_011513408.1:p.Glu155Asp
XM_011515107.1:c.279G>C	XP_011513409.1:p.Glu93Asp
XM_011515108.1:c.201G>C	XP_011513410.1:p.Glu67Asp
XM_011515109.1:c.162G>C	XP_011513411.1:p.Glu54Asp
XM_011515110.1:c.123G>C	XP_011513412.1:p.Glu41Asp
XM_011515111.1:c.96G>C	XP_011513413.1:p.Glu32Asp
XM_011515112.1:c.504G>C	XP_011513414.1:p.Glu168Asp
XM_011515105.2:c.504G>C	XP_011513407.1:p.Glu168Asp
XM_011515106.2:c.465G>C	XP_011513408.1:p.Glu155Asp
XM_011515107.2:c.279G>C	XP_011513409.1:p.Glu93Asp
XM_017011721.1:c.522G>C	XP_016867210.1:p.Glu174Asp
XM_017011722.1:c.297G>C	XP_016867211.1:p.Glu99Asp
NM_004067.4:c.201G>C MANE Select	NP_004058.1:p.Glu67Asp
NM_001293070.2:c.240G>C	NP_001279999.1:p.Glu80Asp
NM_001293071.2:c.96G>C	NP_001280000.1:p.Glu32Asp
NM_001293072.2:c.156G>C	NP_001280001.1:p.Glu52Asp
NM_001398427.1:c.-238G>C	NP_001385356.1:n.-238G>C