Canonical Allele Identifier: CA2763875378
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.144559417_144559418del , CM000666.2:g.144559417_144559418del GRCh38
NC_000004.11:g.145480569_145480570del , CM000666.1:g.145480569_145480570del GRCh37
NC_000004.10:g.145700019_145700020del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000649263.1:c.328-143436_328-143435del ENSP00000497507.1:n.328-143436_328-143435del
XR_939272.1:n.178+2570_178+2571del
XR_939273.1:n.178+2570_178+2571del
XR_939272.2:n.522+2570_522+2571del
XR_939273.2:n.522+2570_522+2571del