Canonical Allele Identifier: CA2750862389

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88859368_88859369insTTTTTT , CM000664.2:g.88859368_88859369insTTTTTT GRCh38
NC_000002.11:g.89158881_89158882insTTTTTT , CM000664.1:g.89158881_89158882insTTTTTT GRCh37
NC_000002.10:g.88939996_88939997insTTTTTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377423.6:c.389-1682_389-1681insAAAAAA (IGKV1-12) ENSP00000480537.2:n.389-1682_389-1681insA...
ENST00000430694.5:c.37+1521_37+1522insAAAAAA (IGKC) ENSP00000481923.2:n.37+1521_37+1522insAAA...
ENST00000610638.3:c.398-1682_398-1681insAAAAAA (IGKC) ENSP00000484499.3:n.398-1682_398-1681insA...
ENST00000634828.1:c.383-1682_383-1681insAAAAAA (IGKV1-8) ENSP00000489500.1:n.383-1682_383-1681insA...