Canonical Allele Identifier: CA915940393

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.113129452_113129612del , CM000675.2:g.113129452_113129612del GRCh38
NC_000013.10:g.113783766_113783926del , CM000675.1:g.113783766_113783926del GRCh37
NC_000013.9:g.112831767_112831927del NCBI36
NG_009258.1:g.11654_11814del , LRG_548:g.11654_11814del

Transcript Alleles

HGVS Amino-acid change
ENST00000375559.8:c.71_231del (F10)
ENST00000375551.7:c.71_231del (F10)
ENST00000375559.7:c.71_231del (F10)
ENST00000409306.5:c.71_231del (F10)
ENST00000410083.6:c.71_231del (F10)
ENST00000477269.5:n.108_268del (F10)
ENST00000483537.1:n.91_251del (F10)
NM_000504.3:c.71_231del , LRG_548t1:c.71_231del (F10)
NM_001312674.1:c.71_231del (F10)
NM_001312675.1:c.71_231del (F10)
NR_126424.1:n.41+395_41+555del (F10-AS1)
NM_000504.4:c.71_231del (F10)
NM_001312674.2:c.71_231del (F10)
NM_001312675.2:c.71_231del (F10)