Canonical Allele Identifier: CA1760507875

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.5907561_5907570delinsGAGGAAAGGA , CM000670.2:g.5907561_5907570delinsGAGGAAAGGA	GRCh38
NC_000008.10:g.5765083_5765092delinsGAGGAAAGGA , CM000670.1:g.5765083_5765092delinsGAGGAAAGGA	GRCh37
NC_000008.9:g.5752491_5752500delinsGAGGAAAGGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_941374.1:n.308-7839_308-7830delinsTCCTTTCCTC
XR_941375.1:n.308-7839_308-7830delinsTCCTTTCCTC
XR_941376.1:n.406-7839_406-7830delinsTCCTTTCCTC
XR_941377.1:n.308-7839_308-7830delinsTCCTTTCCTC
XR_941378.1:n.216-7839_216-7830delinsTCCTTTCCTC
XR_001745765.1:n.308-7839_308-7830delinsTCCTTTCCTC
XR_001745766.1:n.406-7839_406-7830delinsTCCTTTCCTC
XR_001745767.1:n.216-7839_216-7830delinsTCCTTTCCTC
XR_001745768.1:n.308-7839_308-7830delinsTCCTTTCCTC
XR_941374.2:n.308-7839_308-7830delinsTCCTTTCCTC
XR_941375.2:n.308-7839_308-7830delinsTCCTTTCCTC