Canonical Allele Identifier: CA376947151
Gene: NODAL HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.72201377A>T (hg19) chr10:g.70441621A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70441621A>T , CM000672.2:g.70441621A>T GRCh38
NC_000010.10:g.72201377A>T , CM000672.1:g.72201377A>T GRCh37
NC_000010.9:g.71871383A>T NCBI36
NG_012448.1:g.5089T>A
NG_012448.2:g.11328T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000287139.8:c.47T>A MANE Select ENSP00000287139.3:p.Leu16Gln
ENST00000287139.7:c.47T>A ENSP00000287139.3:p.Leu16Gln
ENST00000414871.1:c.29-5638T>A ENSP00000394468.1:n.29-5638T>A
NM_018055.4:c.47T>A NP_060525.3:p.Leu16Gln
NM_001329906.1:c.-206-5638T>A NP_001316835.1:n.-206-5638T>A
XM_024448028.1:c.-207+410T>A XP_024303796.1:n.-207+410T>A
NM_018055.5:c.47T>A MANE Select NP_060525.3:p.Leu16Gln
NM_001329906.2:c.-206-5638T>A NP_001316835.1:n.-206-5638T>A
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