Canonical Allele Identifier: CA2499995773

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232545867del , CM000664.2:g.232545867del GRCh38
NC_000002.11:g.233410577del , CM000664.1:g.233410577del GRCh37
NC_000002.10:g.233118821del NCBI36
NG_012954.1:g.11141del
NG_012954.2:g.11176del

Transcript Alleles

HGVS Amino-acid Change
ENST00000408957.7:c.*2243del (TIGD1) MANE Select ENSP00000386186.3:n.*2243del
ENST00000651502.1:c.*151del (CHRNG) MANE Select ENSP00000498757.1:n.*151del
ENST00000389494.7:c.*151del (CHRNG) ENSP00000374145.3:n.*151del
NM_005199.4:c.*151del (CHRNG) NP_005190.4:n.*151del
NM_005199.5:c.*151del (CHRNG) MANE Select NP_005190.4:n.*151del
NM_145702.4:c.*2243del (TIGD1) MANE Select NP_663748.1:n.*2243del