Canonical Allele Identifier: CA1335319356
Gene: TIGD1 HGNC NCBI
CHRNG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.232546306_232546311delinsCTCTTT , CM000664.2:g.232546306_232546311delinsCTCTTT GRCh38
NC_000002.11:g.233411016_233411021delinsCTCTTT , CM000664.1:g.233411016_233411021delinsCTCTTT GRCh37
NC_000002.10:g.233119260_233119265delinsCTCTTT NCBI36
NG_012954.1:g.11580_11585delinsCTCTTT
NG_012954.2:g.11615_11620delinsCTCTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000408957.7:c.*1796_*1801delinsAAAGAG (TIGD1) MANE Select ENSP00000386186.3:n.*1796_*1801delinsAAAGAG
ENST00000651502.1:c.*590_*595delinsCTCTTT (CHRNG) MANE Select ENSP00000498757.1:n.*590_*595delinsCTCTTT
ENST00000389494.7:c.*590_*595delinsCTCTTT (CHRNG) ENSP00000374145.3:n.*590_*595delinsCTCTTT
NM_005199.4:c.*590_*595delinsCTCTTT (CHRNG) NP_005190.4:n.*590_*595delinsCTCTTT
NM_005199.5:c.*590_*595delinsCTCTTT (CHRNG) MANE Select NP_005190.4:n.*590_*595delinsCTCTTT
NM_145702.4:c.*1796_*1801delinsAAAGAG (TIGD1) MANE Select NP_663748.1:n.*1796_*1801delinsAAAGAG
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