Canonical Allele Identifier: CA1276913289
Gene: NCK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.105886170C= , CM000664.2:g.105886170C= GRCh38
NC_000002.11:g.106502626C= , CM000664.1:g.106502626C= GRCh37
NC_000002.10:g.105869058C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000233154.9:c.948+4121C= MANE Select ENSP00000233154.4:n.948+4121C=
ENST00000233154.8:c.948+4121C= ENSP00000233154.4:n.948+4121C=
ENST00000393349.2:c.948+4121C= ENSP00000377018.2:n.948+4121C=
ENST00000451463.6:c.227-6812C= ENSP00000410428.2:n.227-6812C=
ENST00000522586.5:c.227-6812C= ENSP00000431109.1:n.227-6812C=
NM_001004720.2:c.948+4121C= NP_001004720.1:n.948+4121C=
NM_001004722.3:c.227-6812C= NP_001004722.1:n.227-6812C=
NM_003581.4:c.948+4121C= NP_003572.2:n.948+4121C=
XM_006712797.2:c.948+4121C= XP_006712860.1:n.948+4121C=
XM_011511991.1:c.948+4121C= XP_011510293.1:n.948+4121C=
XM_011511992.1:c.234-6812C= XP_011510294.1:n.234-6812C=
XM_006712797.3:c.948+4121C= XP_006712860.1:n.948+4121C=
XM_011511991.3:c.948+4121C= XP_011510293.1:n.948+4121C=
XM_011511992.2:c.227-6812C= XP_011510294.2:n.227-6812C=
XM_017005103.1:c.948+4121C= XP_016860592.1:n.948+4121C=
XM_017005104.1:c.948+4121C= XP_016860593.1:n.948+4121C=
XM_017005105.1:c.948+4121C= XP_016860594.1:n.948+4121C=
NM_003581.5:c.948+4121C= MANE Select NP_003572.2:n.948+4121C=
NM_001004720.3:c.948+4121C= NP_001004720.1:n.948+4121C=
NM_001004722.4:c.227-6812C= NP_001004722.1:n.227-6812C=