Canonical Allele Identifier: CA2754657536

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232546328_232546329insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.2:g.232546328_232546329insTTTTTTTTTTTTTTTTTTTTTTTTT GRCh38
NC_000002.11:g.233411038_233411039insTTTTTTTTTTTTTTTTTTTTTTTTT , CM000664.1:g.233411038_233411039insTTTTTTTTTTTTTTTTTTTTTTTTT GRCh37
NC_000002.10:g.233119282_233119283insTTTTTTTTTTTTTTTTTTTTTTTTT NCBI36
NG_012954.1:g.11602_11603insTTTTTTTTTTTTTTTTTTTTTTTTT
NG_012954.2:g.11637_11638insTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000408957.7:c.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA (TIGD1) MANE Select ENSP00000386186.3:n.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA
ENST00000651502.1:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT (CHRNG) MANE Select ENSP00000498757.1:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000389494.7:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT (CHRNG) ENSP00000374145.3:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_005199.5:c.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT (CHRNG) MANE Select NP_005190.4:n.*612_*613insTTTTTTTTTTTTTTTTTTTTTTTTT
NM_145702.4:c.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA (TIGD1) MANE Select NP_663748.1:n.*1798_*1799insAAAAAAAAAAAAAAAAAAAAAAAAA