Canonical Allele Identifier: CA9132732

Gene: VAV1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6833972C>T , CM000681.2:g.6833972C>T	GRCh38
NC_000019.9:g.6833983C>T , CM000681.1:g.6833983C>T	GRCh37
NC_000019.8:g.6784983C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602142.6:c.1777+19C>T MANE Select	ENSP00000472929.1:n.1777+19C>T
ENST00000304076.6:c.1777+19C>T	ENSP00000302269.2:n.1777+19C>T
ENST00000539284.2:c.1609+19C>T	ENSP00000443242.2:n.1609+19C>T
ENST00000596764.5:c.1681+19C>T	ENSP00000469450.1:n.1681+19C>T
ENST00000599806.5:c.1612+19C>T	ENSP00000472803.1:n.1612+19C>T
ENST00000602142.5:c.1777+19C>T	ENSP00000472929.1:n.1777+19C>T
NM_001258206.1:c.1777+19C>T	NP_001245135.1:n.1777+19C>T
NM_001258207.1:c.1681+19C>T	NP_001245136.1:n.1681+19C>T
NM_005428.3:c.1777+19C>T	NP_005419.2:n.1777+19C>T
XM_005259642.1:c.1777+19C>T	XP_005259699.1:n.1777+19C>T
XM_011528254.1:c.520+19C>T	XP_011526556.1:n.520+19C>T
NM_005428.4:c.1777+19C>T MANE Select	NP_005419.2:n.1777+19C>T
NM_001258206.2:c.1777+19C>T	NP_001245135.1:n.1777+19C>T
NM_001258207.2:c.1681+19C>T	NP_001245136.1:n.1681+19C>T