Canonical Allele Identifier: CA2540175634

Gene: NCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.105886176G>T , CM000664.2:g.105886176G>T	GRCh38
NC_000002.11:g.106502632G>T , CM000664.1:g.106502632G>T	GRCh37
NC_000002.10:g.105869064G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000233154.9:c.948+4127G>T MANE Select	ENSP00000233154.4:n.948+4127G>T
ENST00000233154.8:c.948+4127G>T	ENSP00000233154.4:n.948+4127G>T
ENST00000393349.2:c.948+4127G>T	ENSP00000377018.2:n.948+4127G>T
ENST00000451463.6:c.227-6806G>T	ENSP00000410428.2:n.227-6806G>T
ENST00000522586.5:c.227-6806G>T	ENSP00000431109.1:n.227-6806G>T
NM_001004720.2:c.948+4127G>T	NP_001004720.1:n.948+4127G>T
NM_001004722.3:c.227-6806G>T	NP_001004722.1:n.227-6806G>T
NM_003581.4:c.948+4127G>T	NP_003572.2:n.948+4127G>T
XM_006712797.2:c.948+4127G>T	XP_006712860.1:n.948+4127G>T
XM_011511991.1:c.948+4127G>T	XP_011510293.1:n.948+4127G>T
XM_011511992.1:c.234-6806G>T	XP_011510294.1:n.234-6806G>T
XM_006712797.3:c.948+4127G>T	XP_006712860.1:n.948+4127G>T
XM_011511991.3:c.948+4127G>T	XP_011510293.1:n.948+4127G>T
XM_011511992.2:c.227-6806G>T	XP_011510294.2:n.227-6806G>T
XM_017005103.1:c.948+4127G>T	XP_016860592.1:n.948+4127G>T
XM_017005104.1:c.948+4127G>T	XP_016860593.1:n.948+4127G>T
XM_017005105.1:c.948+4127G>T	XP_016860594.1:n.948+4127G>T
NM_003581.5:c.948+4127G>T MANE Select	NP_003572.2:n.948+4127G>T
NM_001004720.3:c.948+4127G>T	NP_001004720.1:n.948+4127G>T
NM_001004722.4:c.227-6806G>T	NP_001004722.1:n.227-6806G>T