Canonical Allele Identifier: CA16609410
Gene: VAC14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.70697199G>A , CM000678.2:g.70697199G>A GRCh38
NC_000016.9:g.70731102G>A , CM000678.1:g.70731102G>A GRCh37
NC_000016.8:g.69288603G>A NCBI36
NG_054902.1:g.108971C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261776.10:c.1895C>T MANE Select ENSP00000261776.5:p.Thr632Met
ENST00000261776.9:c.1895C>T ENSP00000261776.5:p.Thr632Met
ENST00000536184.6:c.191C>T ENSP00000439284.2:p.Thr64Met
ENST00000564685.5:n.583C>T
ENST00000566416.1:c.467-26C>T
ENST00000568548.5:c.*1621C>T ENSP00000454650.1:n.*1621C>T
ENST00000568886.5:c.*520C>T ENSP00000457809.1:n.*520C>T
NM_018052.3:c.1895C>T NP_060522.3:p.Thr632Met
XM_005256038.2:c.1895C>T XP_005256095.1:p.Thr632Met
NM_001351157.1:c.1193C>T NP_001338086.1:p.Thr398Met
NM_018052.4:c.1895C>T NP_060522.3:p.Thr632Met
XM_005256038.4:c.1895C>T XP_005256095.1:p.Thr632Met
NM_018052.5:c.1895C>T MANE Select NP_060522.3:p.Thr632Met
NM_001351157.2:c.1193C>T NP_001338086.1:p.Thr398Met