Canonical Allele Identifier: CA1244361
Community Standard Title: NM_003762.5(VAMP4):c.404T>C (p.Ile135Thr)
Gene: VAMP4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.171704528A>G , CM000663.2:g.171704528A>G GRCh38
NC_000001.10:g.171673668A>G , CM000663.1:g.171673668A>G GRCh37
NC_000001.9:g.169940291A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003762.5:c.404T>C MANE Select NP_003753.2:p.Ile135Thr
ENST00000236192.12:c.404T>C MANE Select ENSP00000236192.7:p.Ile135Thr
NM_001185127.1:c.401T>C NP_001172056.1:p.Ile134Thr
NM_001185127.2:c.401T>C NP_001172056.1:p.Ile134Thr
NM_003762.4:c.404T>C NP_003753.2:p.Ile135Thr
NR_033704.1:n.783T>C
NR_033704.2:n.609T>C
ENST00000236192.11:c.404T>C ENSP00000236192.7:p.Ile135Thr
ENST00000367740.2:c.401T>C ENSP00000356714.2:p.Ile134Thr
ENST00000474047.5:c.404T>C ENSP00000435933.1:p.Ile135Thr
ENST00000482519.1:n.563T>C
XM_017002713.2:c.*55T>C XP_016858202.1:n.*55T>C
XR_426805.1:n.641T>C