Canonical Allele Identifier: CA449649784

Gene: HCP5

Linked Data

• MyVariant Identifiers: chr6:g.31431587_31431588insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31463810_31463811insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT , CM000668.2:g.31463810_31463811insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT	GRCh38
NC_000006.11:g.31431587_31431588insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT , CM000668.1:g.31431587_31431588insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT	GRCh37
NC_000006.10:g.31539566_31539567insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040662.1:n.540_541insCGAGCAGCGAAATAAATAGCCAAAAAATAAAAAACTACAACATAAT