Canonical Allele Identifier: CA9132621

Gene: VAV1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6833199G>A , CM000681.2:g.6833199G>A	GRCh38
NC_000019.9:g.6833210G>A , CM000681.1:g.6833210G>A	GRCh37
NC_000019.8:g.6784210G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602142.6:c.1524G>A MANE Select	ENSP00000472929.1:p.Pro508=
ENST00000304076.6:c.1524G>A	ENSP00000302269.2:p.Pro508=
ENST00000539284.2:c.1356G>A	ENSP00000443242.2:p.Pro452=
ENST00000596764.5:c.1428G>A	ENSP00000469450.1:p.Pro476=
ENST00000599806.5:c.1359G>A	ENSP00000472803.1:p.Pro453=
ENST00000600396.1:n.505G>A
ENST00000601452.5:n.608G>A
ENST00000602142.5:c.1524G>A	ENSP00000472929.1:p.Pro508=
NM_001258206.1:c.1524G>A	NP_001245135.1:p.Pro508=
NM_001258207.1:c.1428G>A	NP_001245136.1:p.Pro476=
NM_005428.3:c.1524G>A	NP_005419.2:p.Pro508=
XM_005259642.1:c.1524G>A	XP_005259699.1:p.Pro508=
XM_011528254.1:c.267G>A	XP_011526556.1:p.Pro89=
NM_005428.4:c.1524G>A MANE Select	NP_005419.2:p.Pro508=
NM_001258206.2:c.1524G>A	NP_001245135.1:p.Pro508=
NM_001258207.2:c.1428G>A	NP_001245136.1:p.Pro476=