Canonical Allele Identifier: CA367241780

Gene: CHN2

Linked Data

• MyVariant Identifiers: chr7:g.29438086T>C (hg19) ; chr7:g.29398470T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398470T>C , CM000669.2:g.29398470T>C	GRCh38
NC_000007.13:g.29438086T>C , CM000669.1:g.29438086T>C	GRCh37
NC_000007.12:g.29404611T>C	NCBI36
NG_029365.2:g.256924T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.313T>C	ENSP00000386968.2:p.Tyr105His
ENST00000439384.6:n.536T>C
ENST00000446446.6:c.274T>C	ENSP00000396867.2:p.Tyr92His
ENST00000706158.1:c.*218T>C	ENSP00000516236.1:n.*218T>C
ENST00000706159.1:c.186T>C	ENSP00000516237.1:p.Ala62=
ENST00000706160.1:c.274T>C	ENSP00000516238.1:p.Tyr92His
ENST00000706161.1:c.352T>C	ENSP00000516239.1:p.Tyr118His
ENST00000706162.1:c.274T>C	ENSP00000516240.1:p.Tyr92His
ENST00000706163.1:c.50-81809T>C	ENSP00000516241.1:n.50-81809T>C
ENST00000222792.11:c.274T>C MANE Select	ENSP00000222792.7:p.Tyr92His
ENST00000644824.1:c.499T>C	ENSP00000495614.1:p.Tyr167His
ENST00000222792.10:c.274T>C	ENSP00000222792.6:p.Tyr92His
ENST00000409350.5:c.313T>C	ENSP00000386968.1:p.Tyr105His
ENST00000409922.5:n.485T>C
ENST00000409964.6:n.473T>C
ENST00000412536.5:n.294T>C
ENST00000435288.6:c.168+4768T>C	ENSP00000400282.3:n.168+4768T>C
ENST00000439384.5:c.499T>C	ENSP00000409843.1:p.Tyr167His
ENST00000474070.5:c.374T>C
ENST00000478128.6:n.368T>C
ENST00000482820.6:n.483T>C
ENST00000491856.1:n.1823T>C
ENST00000495789.6:c.274T>C	ENSP00000438587.2:p.Tyr92His
ENST00000539389.5:c.274T>C	ENSP00000440526.2:p.Tyr92His
ENST00000539406.5:c.274T>C	ENSP00000444063.2:p.Tyr92His
NM_001293069.1:c.499T>C	NP_001279998.1:p.Tyr167His
NM_001293070.1:c.313T>C	NP_001279999.1:p.Tyr105His
NM_001293071.1:c.169T>C	NP_001280000.1:p.Tyr57His
NM_001293072.1:c.229T>C	NP_001280001.1:p.Tyr77His
NM_004067.3:c.274T>C	NP_004058.1:p.Tyr92His
XM_011515105.1:c.577T>C	XP_011513407.1:p.Tyr193His
XM_011515106.1:c.538T>C	XP_011513408.1:p.Tyr180His
XM_011515107.1:c.352T>C	XP_011513409.1:p.Tyr118His
XM_011515108.1:c.274T>C	XP_011513410.1:p.Tyr92His
XM_011515109.1:c.235T>C	XP_011513411.1:p.Tyr79His
XM_011515110.1:c.196T>C	XP_011513412.1:p.Tyr66His
XM_011515111.1:c.169T>C	XP_011513413.1:p.Tyr57His
XM_011515112.1:c.577T>C	XP_011513414.1:p.Tyr193His
XM_011515105.2:c.577T>C	XP_011513407.1:p.Tyr193His
XM_011515106.2:c.538T>C	XP_011513408.1:p.Tyr180His
XM_011515107.2:c.352T>C	XP_011513409.1:p.Tyr118His
XM_017011721.1:c.595T>C	XP_016867210.1:p.Tyr199His
XM_017011722.1:c.370T>C	XP_016867211.1:p.Tyr124His
NM_004067.4:c.274T>C MANE Select	NP_004058.1:p.Tyr92His
NM_001293070.2:c.313T>C	NP_001279999.1:p.Tyr105His
NM_001293071.2:c.169T>C	NP_001280000.1:p.Tyr57His
NM_001293072.2:c.229T>C	NP_001280001.1:p.Tyr77His
NM_001398427.1:c.-165T>C	NP_001385356.1:n.-165T>C