Canonical Allele Identifier: CA534824051

Gene: NCK2

Linked Data

• dbSNP Id: rs1359377717
• gnomAD v2: 2-106502609-T-C
• gnomAD v3: 2-105886153-T-C
• gnomAD v4: 2-105886153-T-C
• MyVariant Identifiers: chr2:g.106502609T>C (hg19) ; chr2:g.105886153T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.105886153T>C , CM000664.2:g.105886153T>C	GRCh38
NC_000002.11:g.106502609T>C , CM000664.1:g.106502609T>C	GRCh37
NC_000002.10:g.105869041T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233154.9:c.948+4104T>C MANE Select	ENSP00000233154.4:n.948+4104T>C
ENST00000233154.8:c.948+4104T>C	ENSP00000233154.4:n.948+4104T>C
ENST00000393349.2:c.948+4104T>C	ENSP00000377018.2:n.948+4104T>C
ENST00000451463.6:c.227-6829T>C	ENSP00000410428.2:n.227-6829T>C
ENST00000522586.5:c.227-6829T>C	ENSP00000431109.1:n.227-6829T>C
NM_001004720.2:c.948+4104T>C	NP_001004720.1:n.948+4104T>C
NM_001004722.3:c.227-6829T>C	NP_001004722.1:n.227-6829T>C
NM_003581.4:c.948+4104T>C	NP_003572.2:n.948+4104T>C
XM_006712797.2:c.948+4104T>C	XP_006712860.1:n.948+4104T>C
XM_011511991.1:c.948+4104T>C	XP_011510293.1:n.948+4104T>C
XM_011511992.1:c.234-6829T>C	XP_011510294.1:n.234-6829T>C
XM_006712797.3:c.948+4104T>C	XP_006712860.1:n.948+4104T>C
XM_011511991.3:c.948+4104T>C	XP_011510293.1:n.948+4104T>C
XM_011511992.2:c.227-6829T>C	XP_011510294.2:n.227-6829T>C
XM_017005103.1:c.948+4104T>C	XP_016860592.1:n.948+4104T>C
XM_017005104.1:c.948+4104T>C	XP_016860593.1:n.948+4104T>C
XM_017005105.1:c.948+4104T>C	XP_016860594.1:n.948+4104T>C
NM_003581.5:c.948+4104T>C MANE Select	NP_003572.2:n.948+4104T>C
NM_001004720.3:c.948+4104T>C	NP_001004720.1:n.948+4104T>C
NM_001004722.4:c.227-6829T>C	NP_001004722.1:n.227-6829T>C