Canonical Allele Identifier: CA1500737489

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144559216_144559219delinsATCT , CM000666.2:g.144559216_144559219delinsATCT	GRCh38
NC_000004.11:g.145480368_145480371delinsATCT , CM000666.1:g.145480368_145480371delinsATCT	GRCh37
NC_000004.10:g.145699818_145699821delinsATCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-143241_328-143238delinsAGAT	ENSP00000497507.1:n.328-143241_328-143238delinsAGAT
XR_939272.1:n.178+2765_178+2768delinsAGAT
XR_939273.1:n.178+2765_178+2768delinsAGAT
XR_939272.2:n.522+2765_522+2768delinsAGAT
XR_939273.2:n.522+2765_522+2768delinsAGAT