Canonical Allele Identifier: CA2820657038
Gene: NDP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949610_43949611insTCTTT , CM000685.2:g.43949610_43949611insTCTTT GRCh38
NC_000023.10:g.43808856_43808857insTCTTT , CM000685.1:g.43808856_43808857insTCTTT GRCh37
NC_000023.9:g.43693800_43693801insTCTTT NCBI36
NG_009832.1:g.29066_29067insAAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.*189_*190insAAGAA MANE Select ENSP00000495972.1:n.*189_*190insAAGAA
ENST00000647044.1:c.*189_*190insAAGAA ENSP00000495811.1:n.*189_*190insAAGAA
ENST00000378062.5:c.*189_*190insAAGAA ENSP00000367301.5:n.*189_*190insAAGAA
NM_000266.3:c.*189_*190insAAGAA NP_000257.1:n.*189_*190insAAGAA
NM_000266.4:c.*189_*190insAAGAA MANE Select NP_000257.1:n.*189_*190insAAGAA