Canonical Allele Identifier: CA365352198

Gene: WASF1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.110108660A>G , CM000668.2:g.110108660A>G	GRCh38
NC_000006.11:g.110429863A>G , CM000668.1:g.110429863A>G	GRCh37
NC_000006.10:g.110536556A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392589.6:c.290T>C MANE Select	ENSP00000376368.1:p.Met97Thr
ENST00000265601.7:c.290T>C	ENSP00000265601.3:p.Met97Thr
ENST00000359451.6:c.290T>C	ENSP00000352425.2:p.Met97Thr
ENST00000368938.5:c.290T>C	ENSP00000357934.1:p.Met97Thr
ENST00000392586.5:c.290T>C	ENSP00000376365.1:p.Met97Thr
ENST00000392587.6:c.290T>C	ENSP00000376366.2:p.Met97Thr
ENST00000392588.5:c.290T>C	ENSP00000376367.1:p.Met97Thr
ENST00000392589.5:c.290T>C	ENSP00000376368.1:p.Met97Thr
ENST00000444391.5:c.290T>C	ENSP00000407041.1:p.Met97Thr
NM_001024934.1:c.290T>C	NP_001020105.1:p.Met97Thr
NM_001024935.1:c.290T>C	NP_001020106.1:p.Met97Thr
NM_001024936.1:c.290T>C	NP_001020107.1:p.Met97Thr
NM_003931.2:c.290T>C	NP_003922.1:p.Met97Thr
XM_005267203.3:c.290T>C	XP_005267260.1:p.Met97Thr
XM_005267204.2:c.290T>C	XP_005267261.1:p.Met97Thr
XM_005267205.2:c.290T>C	XP_005267262.1:p.Met97Thr
XM_005267206.2:c.290T>C	XP_005267263.1:p.Met97Thr
XM_005267207.2:c.290T>C	XP_005267264.1:p.Met97Thr
XM_011536233.1:c.290T>C	XP_011534535.1:p.Met97Thr
XM_011536234.1:c.290T>C	XP_011534536.1:p.Met97Thr
XM_011536235.1:c.290T>C	XP_011534537.1:p.Met97Thr
NM_003931.3:c.290T>C MANE Select	NP_003922.1:p.Met97Thr
NM_001024934.2:c.290T>C	NP_001020105.1:p.Met97Thr
NM_001024935.2:c.290T>C	NP_001020106.1:p.Met97Thr
NM_001024936.2:c.290T>C	NP_001020107.1:p.Met97Thr