Canonical Allele Identifier: CA9132880

Gene: VAV1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6850701A>T , CM000681.2:g.6850701A>T	GRCh38
NC_000019.9:g.6850712A>T , CM000681.1:g.6850712A>T	GRCh37
NC_000019.8:g.6801712A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000602142.6:c.2161A>T MANE Select	ENSP00000472929.1:p.Met721Leu
ENST00000304076.6:c.2095A>T	ENSP00000302269.2:p.Met699Leu
ENST00000539284.2:c.1993A>T	ENSP00000443242.2:p.Met665Leu
ENST00000596764.5:c.2065A>T	ENSP00000469450.1:p.Met689Leu
ENST00000599806.5:c.1996A>T	ENSP00000472803.1:p.Met666Leu
ENST00000602142.5:c.2161A>T	ENSP00000472929.1:p.Met721Leu
NM_001258206.1:c.2095A>T	NP_001245135.1:p.Met699Leu
NM_001258207.1:c.2065A>T	NP_001245136.1:p.Met689Leu
NM_005428.3:c.2161A>T	NP_005419.2:p.Met721Leu
XM_005259642.1:c.2161A>T	XP_005259699.1:p.Met721Leu
XM_011528254.1:c.904A>T	XP_011526556.1:p.Met302Leu
NM_005428.4:c.2161A>T MANE Select	NP_005419.2:p.Met721Leu
NM_001258206.2:c.2095A>T	NP_001245135.1:p.Met699Leu
NM_001258207.2:c.2065A>T	NP_001245136.1:p.Met689Leu