Canonical Allele Identifier: CA754638734

Gene: NCK2

Linked Data

• dbSNP Id: rs1393080724
• MyVariant Identifiers: chr2:g.106502645T>A (hg19) ; chr2:g.105886189T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.105886189T>A , CM000664.2:g.105886189T>A	GRCh38
NC_000002.11:g.106502645T>A , CM000664.1:g.106502645T>A	GRCh37
NC_000002.10:g.105869077T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233154.9:c.948+4140T>A MANE Select	ENSP00000233154.4:n.948+4140T>A
ENST00000233154.8:c.948+4140T>A	ENSP00000233154.4:n.948+4140T>A
ENST00000393349.2:c.948+4140T>A	ENSP00000377018.2:n.948+4140T>A
ENST00000451463.6:c.227-6793T>A	ENSP00000410428.2:n.227-6793T>A
ENST00000522586.5:c.227-6793T>A	ENSP00000431109.1:n.227-6793T>A
NM_001004720.2:c.948+4140T>A	NP_001004720.1:n.948+4140T>A
NM_001004722.3:c.227-6793T>A	NP_001004722.1:n.227-6793T>A
NM_003581.4:c.948+4140T>A	NP_003572.2:n.948+4140T>A
XM_006712797.2:c.948+4140T>A	XP_006712860.1:n.948+4140T>A
XM_011511991.1:c.948+4140T>A	XP_011510293.1:n.948+4140T>A
XM_011511992.1:c.234-6793T>A	XP_011510294.1:n.234-6793T>A
XM_006712797.3:c.948+4140T>A	XP_006712860.1:n.948+4140T>A
XM_011511991.3:c.948+4140T>A	XP_011510293.1:n.948+4140T>A
XM_011511992.2:c.227-6793T>A	XP_011510294.2:n.227-6793T>A
XM_017005103.1:c.948+4140T>A	XP_016860592.1:n.948+4140T>A
XM_017005104.1:c.948+4140T>A	XP_016860593.1:n.948+4140T>A
XM_017005105.1:c.948+4140T>A	XP_016860594.1:n.948+4140T>A
NM_003581.5:c.948+4140T>A MANE Select	NP_003572.2:n.948+4140T>A
NM_001004720.3:c.948+4140T>A	NP_001004720.1:n.948+4140T>A
NM_001004722.4:c.227-6793T>A	NP_001004722.1:n.227-6793T>A