Canonical Allele Identifier: CA1605795074

Gene:

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.1535834_1535838delinsCCTTT , CM000668.2:g.1535834_1535838delinsCCTTT	GRCh38
NC_000006.11:g.1536069_1536073delinsCCTTT , CM000668.1:g.1536069_1536073delinsCCTTT	GRCh37
NC_000006.10:g.1481068_1481072delinsCCTTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_427861.2:n.234+16508_234+16512delinsAAAGG
XR_926380.1:n.218-2622_218-2618delinsCCTTT
XR_926381.1:n.1108-2622_1108-2618delinsCCTTT
XR_926382.1:n.235-6659_235-6655delinsAAAGG
XR_926384.1:n.200-6659_200-6655delinsAAAGG
XR_001743921.1:n.235-6683_235-6679delinsAAAGG
XR_427861.3:n.234+16508_234+16512delinsAAAGG
XR_926381.2:n.1123-2622_1123-2618delinsCCTTT