Canonical Allele Identifier: CA410322387
Gene: RIPK4 HGNC NCBI

Linked Data

gnomAD v4: 21-41756610-T-C
MyVariant Identifiers: chr21:g.43176770T>C (hg19) chr21:g.41756610T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.41756610T>C , CM000683.2:g.41756610T>C GRCh38
NC_000021.8:g.43176770T>C , CM000683.1:g.43176770T>C GRCh37
NC_000021.7:g.42049839T>C NCBI36
NG_032113.1:g.15480A>G
NG_032113.2:g.15480A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000332512.8:c.389A>G MANE Select ENSP00000332454.3:p.Asn130Ser
ENST00000332512.7:c.389A>G ENSP00000332454.3:p.Asn130Ser
ENST00000352483.3:c.389A>G ENSP00000330161.2:p.Asn130Ser
NM_020639.2:c.389A>G NP_065690.2:p.Asn130Ser
NM_020639.3:c.389A>G MANE Select NP_065690.2:p.Asn130Ser
Search 100 bp 5'
Search 100 bp 3'