Canonical Allele Identifier: CA156540701

Gene: CHN2

Linked Data

• dbSNP Id: rs58159203
• gnomAD v2: 7-29437673-AAGGG-A
• gnomAD v3: 7-29398057-AAGGG-A
• gnomAD v4: 7-29398057-AAGGG-A
• MyVariant Identifiers: chr7:g.29437674_29437677del (hg19) ; chr7:g.29437674_29437678delinsG (hg19) ; chr7:g.29398058_29398061del (hg38) ; chr7:g.29398058_29398062delinsG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.29398058_29398061del , CM000669.2:g.29398058_29398061del	GRCh38
NC_000007.13:g.29437674_29437677del , CM000669.1:g.29437674_29437677del	GRCh37
NC_000007.12:g.29404199_29404202del	NCBI36
NG_029365.2:g.256512_256515del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409350.6:c.216-315_216-312del	ENSP00000386968.2:n.216-315_216-312del
ENST00000439384.6:n.439-315_439-312del
ENST00000446446.6:c.177-315_177-312del	ENSP00000396867.2:n.177-315_177-312del
ENST00000706158.1:c.*121-315_*121-312del	ENSP00000516236.1:n.*121-315_*121-312del
ENST00000706159.1:c.89-315_89-312del	ENSP00000516237.1:n.89-315_89-312del
ENST00000706160.1:c.177-315_177-312del	ENSP00000516238.1:n.177-315_177-312del
ENST00000706161.1:c.255-315_255-312del	ENSP00000516239.1:n.255-315_255-312del
ENST00000706162.1:c.177-315_177-312del	ENSP00000516240.1:n.177-315_177-312del
ENST00000706163.1:c.50-82221_50-82218del	ENSP00000516241.1:n.50-82221_50-82218del
ENST00000222792.11:c.177-315_177-312del MANE Select	ENSP00000222792.7:n.177-315_177-312del
ENST00000644824.1:c.402-315_402-312del	ENSP00000495614.1:n.402-315_402-312del
ENST00000222792.10:c.177-315_177-312del	ENSP00000222792.6:n.177-315_177-312del
ENST00000409350.5:c.216-315_216-312del	ENSP00000386968.1:n.216-315_216-312del
ENST00000409922.5:n.388-315_388-312del
ENST00000409964.6:n.376-315_376-312del
ENST00000412536.5:n.197-315_197-312del
ENST00000435288.6:c.168+4356_168+4359del	ENSP00000400282.3:n.168+4356_168+4359del
ENST00000439384.5:c.402-315_402-312del	ENSP00000409843.1:n.402-315_402-312del
ENST00000474070.5:c.277-315_277-312del
ENST00000478128.6:n.271-315_271-312del
ENST00000482820.6:n.386-315_386-312del
ENST00000491856.1:n.1411_1414del
ENST00000495789.6:c.177-315_177-312del	ENSP00000438587.2:n.177-315_177-312del
ENST00000539389.5:c.177-315_177-312del	ENSP00000440526.2:n.177-315_177-312del
ENST00000539406.5:c.177-315_177-312del	ENSP00000444063.2:n.177-315_177-312del
NM_001293069.1:c.402-315_402-312del	NP_001279998.1:n.402-315_402-312del
NM_001293070.1:c.216-315_216-312del	NP_001279999.1:n.216-315_216-312del
NM_001293071.1:c.72-315_72-312del	NP_001280000.1:n.72-315_72-312del
NM_001293072.1:c.132-315_132-312del	NP_001280001.1:n.132-315_132-312del
NM_004067.3:c.177-315_177-312del	NP_004058.1:n.177-315_177-312del
XM_011515105.1:c.480-315_480-312del	XP_011513407.1:n.480-315_480-312del
XM_011515106.1:c.441-315_441-312del	XP_011513408.1:n.441-315_441-312del
XM_011515107.1:c.255-315_255-312del	XP_011513409.1:n.255-315_255-312del
XM_011515108.1:c.177-315_177-312del	XP_011513410.1:n.177-315_177-312del
XM_011515109.1:c.138-315_138-312del	XP_011513411.1:n.138-315_138-312del
XM_011515110.1:c.99-315_99-312del	XP_011513412.1:n.99-315_99-312del
XM_011515111.1:c.72-315_72-312del	XP_011513413.1:n.72-315_72-312del
XM_011515112.1:c.480-315_480-312del	XP_011513414.1:n.480-315_480-312del
XM_011515105.2:c.480-315_480-312del	XP_011513407.1:n.480-315_480-312del
XM_011515106.2:c.441-315_441-312del	XP_011513408.1:n.441-315_441-312del
XM_011515107.2:c.255-315_255-312del	XP_011513409.1:n.255-315_255-312del
XM_017011721.1:c.498-315_498-312del	XP_016867210.1:n.498-315_498-312del
XM_017011722.1:c.273-315_273-312del	XP_016867211.1:n.273-315_273-312del
NM_004067.4:c.177-315_177-312del MANE Select	NP_004058.1:n.177-315_177-312del
NM_001293070.2:c.216-315_216-312del	NP_001279999.1:n.216-315_216-312del
NM_001293071.2:c.72-315_72-312del	NP_001280000.1:n.72-315_72-312del
NM_001293072.2:c.132-315_132-312del	NP_001280001.1:n.132-315_132-312del
NM_001398427.1:c.-262-315_-262-312del	NP_001385356.1:n.-262-315_-262-312del