Canonical Allele Identifier: CA1875383734
Gene:

Linked Data

dbSNP Id: rs1830022016

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.117796557_117796565del , CM000671.2:g.117796557_117796565del GRCh38
NC_000009.11:g.120558835_120558843del , CM000671.1:g.120558835_120558843del GRCh37
NC_000009.10:g.119598656_119598664del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000646089.2:c.94-51508_94-51500del ENSP00000496197.1:n.94-51508_94-51500del
ENST00000697624.1:n.201-51508_201-51500del
ENST00000697636.1:c.94-51508_94-51500del ENSP00000513366.1:n.94-51508_94-51500del
ENST00000697637.1:c.94-51508_94-51500del ENSP00000513367.1:n.94-51508_94-51500del
ENST00000697664.1:c.*86+29307_*86+29315del ENSP00000513389.1:n.*86+29307_*86+29315del
ENST00000697665.1:c.94-51508_94-51500del ENSP00000513390.1:n.94-51508_94-51500del
ENST00000697666.1:c.141-51508_141-51500del ENSP00000513391.1:n.141-51508_141-51500del
ENST00000642985.1:c.261-51508_261-51500del ENSP00000493686.1:n.261-51508_261-51500del
ENST00000646089.1:c.94-51508_94-51500del ENSP00000496197.1:n.94-51508_94-51500del
ENST00000665764.1:c.94-51508_94-51500del ENSP00000499745.1:n.94-51508_94-51500del
XR_930289.1:n.1628-6424_1628-6416del
XR_001746915.1:n.2244-6424_2244-6416del