Canonical Allele Identifier: CA2695233786

Gene: WAS

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.48688932_48688941del , CM000685.2:g.48688932_48688941del	GRCh38
NC_000023.10:g.48547321_48547330del , CM000685.1:g.48547321_48547330del	GRCh37
NC_000023.9:g.48432265_48432274del	NCBI36
NG_007877.1:g.10136_10145del , LRG_125:g.10136_10145del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474174.2:n.448_457del
ENST00000698625.1:c.1204_1213del	ENSP00000513844.1:p.Pro402AlafsTer?
ENST00000698626.1:c.1204_1213del	ENSP00000513845.1:p.Pro402AlafsTer?
ENST00000698635.1:c.1204_1213del	ENSP00000513850.1:p.Pro402AlafsTer?
ENST00000376701.5:c.1204_1213del MANE Select	ENSP00000365891.4:p.Pro402AlafsTer?
ENST00000376701.4:c.1204_1213del	ENSP00000365891.4:p.Pro402AlafsTer?
ENST00000474174.1:n.448_457del
NM_000377.2:c.1204_1213del , LRG_125t1:c.1204_1213del	NP_000368.1:p.Pro402AlafsTer?
XM_011543977.1:c.1048_1057del	XP_011542279.1:p.Pro350AlafsTer?
XM_011543977.2:c.1048_1057del	XP_011542279.1:p.Pro350AlafsTer?
XM_017029786.1:c.1204_1213del	XP_016885275.1:p.Pro402AlafsTer?
NM_000377.3:c.1204_1213del MANE Select	NP_000368.1:p.Pro402AlafsTer?