Canonical Allele Identifier: CA367241624

Gene: CHN2

Linked Data

• gnomAD v4: 7-29398398-C-T
• MyVariant Identifiers: chr7:g.29438014C>T (hg19) ; chr7:g.29398398C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398398C>T , CM000669.2:g.29398398C>T	GRCh38
NC_000007.13:g.29438014C>T , CM000669.1:g.29438014C>T	GRCh37
NC_000007.12:g.29404539C>T	NCBI36
NG_029365.2:g.256852C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000409350.6:c.241C>T	ENSP00000386968.2:p.Gln81Ter
ENST00000439384.6:n.464C>T
ENST00000446446.6:c.202C>T	ENSP00000396867.2:p.Gln68Ter
ENST00000706158.1:c.*146C>T	ENSP00000516236.1:n.*146C>T
ENST00000706159.1:c.114C>T	ENSP00000516237.1:p.Ser38=
ENST00000706160.1:c.202C>T	ENSP00000516238.1:p.Gln68Ter
ENST00000706161.1:c.280C>T	ENSP00000516239.1:p.Gln94Ter
ENST00000706162.1:c.202C>T	ENSP00000516240.1:p.Gln68Ter
ENST00000706163.1:c.50-81881C>T	ENSP00000516241.1:n.50-81881C>T
ENST00000222792.11:c.202C>T MANE Select	ENSP00000222792.7:p.Gln68Ter
ENST00000644824.1:c.427C>T	ENSP00000495614.1:p.Gln143Ter
ENST00000222792.10:c.202C>T	ENSP00000222792.6:p.Gln68Ter
ENST00000409350.5:c.241C>T	ENSP00000386968.1:p.Gln81Ter
ENST00000409922.5:n.413C>T
ENST00000409964.6:n.401C>T
ENST00000412536.5:n.222C>T
ENST00000435288.6:c.168+4696C>T	ENSP00000400282.3:n.168+4696C>T
ENST00000439384.5:c.427C>T	ENSP00000409843.1:p.Gln143Ter
ENST00000474070.5:c.302C>T
ENST00000478128.6:n.296C>T
ENST00000482820.6:n.411C>T
ENST00000491856.1:n.1751C>T
ENST00000495789.6:c.202C>T	ENSP00000438587.2:p.Gln68Ter
ENST00000539389.5:c.202C>T	ENSP00000440526.2:p.Gln68Ter
ENST00000539406.5:c.202C>T	ENSP00000444063.2:p.Gln68Ter
NM_001293069.1:c.427C>T	NP_001279998.1:p.Gln143Ter
NM_001293070.1:c.241C>T	NP_001279999.1:p.Gln81Ter
NM_001293071.1:c.97C>T	NP_001280000.1:p.Gln33Ter
NM_001293072.1:c.157C>T	NP_001280001.1:p.Gln53Ter
NM_004067.3:c.202C>T	NP_004058.1:p.Gln68Ter
XM_011515105.1:c.505C>T	XP_011513407.1:p.Gln169Ter
XM_011515106.1:c.466C>T	XP_011513408.1:p.Gln156Ter
XM_011515107.1:c.280C>T	XP_011513409.1:p.Gln94Ter
XM_011515108.1:c.202C>T	XP_011513410.1:p.Gln68Ter
XM_011515109.1:c.163C>T	XP_011513411.1:p.Gln55Ter
XM_011515110.1:c.124C>T	XP_011513412.1:p.Gln42Ter
XM_011515111.1:c.97C>T	XP_011513413.1:p.Gln33Ter
XM_011515112.1:c.505C>T	XP_011513414.1:p.Gln169Ter
XM_011515105.2:c.505C>T	XP_011513407.1:p.Gln169Ter
XM_011515106.2:c.466C>T	XP_011513408.1:p.Gln156Ter
XM_011515107.2:c.280C>T	XP_011513409.1:p.Gln94Ter
XM_017011721.1:c.523C>T	XP_016867210.1:p.Gln175Ter
XM_017011722.1:c.298C>T	XP_016867211.1:p.Gln100Ter
NM_004067.4:c.202C>T MANE Select	NP_004058.1:p.Gln68Ter
NM_001293070.2:c.241C>T	NP_001279999.1:p.Gln81Ter
NM_001293071.2:c.97C>T	NP_001280000.1:p.Gln33Ter
NM_001293072.2:c.157C>T	NP_001280001.1:p.Gln53Ter
NM_001398427.1:c.-237C>T	NP_001385356.1:n.-237C>T