Canonical Allele Identifier: CA107748621

Gene:

Linked Data

• dbSNP Id: rs889411358
• MyVariant Identifiers: chr4:g.145480603_145480604insA (hg19) ; chr4:g.144559451_144559452insA (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-143474dup	ENSP00000497507.1:n.328-143474dup
XR_939272.1:n.178+2532dup
XR_939273.1:n.178+2532dup
XR_939272.2:n.522+2532dup
XR_939273.2:n.522+2532dup