Canonical Allele Identifier: CA1500737736

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144559458_144559459delinsAT , CM000666.2:g.144559458_144559459delinsAT	GRCh38
NC_000004.11:g.145480610_145480611delinsAT , CM000666.1:g.145480610_145480611delinsAT	GRCh37
NC_000004.10:g.145700060_145700061delinsAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-143481_328-143480delinsAT	ENSP00000497507.1:n.328-143481_328-143480delinsAT
XR_939272.1:n.178+2525_178+2526delinsAT
XR_939273.1:n.178+2525_178+2526delinsAT
XR_939272.2:n.522+2525_522+2526delinsAT
XR_939273.2:n.522+2525_522+2526delinsAT