Canonical Allele Identifier: CA1694873505
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24283862_24283870delinsTGAAGGAAA , CM000669.2:g.24283862_24283870delinsTGAAGGAAA GRCh38
NC_000007.13:g.24323481_24323489delinsTGAAGGAAA , CM000669.1:g.24323481_24323489delinsTGAAGGAAA GRCh37
NC_000007.12:g.24290006_24290014delinsTGAAGGAAA NCBI36
NG_016148.1:g.4675_4683delinsTGAAGGAAA

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-28171_42-28163delinsTTTCCTTCA XP_016868399.1:n.42-28171_42-28163delinsT...
XM_017012911.1:c.42-28171_42-28163delinsTTTCCTTCA XP_016868400.1:n.42-28171_42-28163delinsT...
XR_001745121.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745122.1:n.345-86841_345-86833delinsTTTCCTTCA
XR_001745123.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745124.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745125.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745126.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745127.1:n.345-28171_345-28163delinsTTTCCTTCA
XR_001745129.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745130.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745131.1:n.473+35487_473+35495delinsTTTCCTTCA
XR_001745132.1:n.473+35487_473+35495delinsTTTCCTTCA