Canonical Allele Identifier: CA512663788

Gene: RIPK4

Linked Data

• MyVariant Identifiers: chr21:g.43176727G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41756567G>C , CM000683.2:g.41756567G>C	GRCh38
NC_000021.8:g.43176727G>C , CM000683.1:g.43176727G>C	GRCh37
NC_000021.7:g.42049796G>C	NCBI36
NG_032113.1:g.15523C>G
NG_032113.2:g.15523C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332512.8:c.432C>G MANE Select	ENSP00000332454.3:p.Leu144=
ENST00000332512.7:c.432C>G	ENSP00000332454.3:p.Leu144=
ENST00000352483.3:c.432C>G	ENSP00000330161.2:p.Leu144=
NM_020639.2:c.432C>G	NP_065690.2:p.Leu144=
NM_020639.3:c.432C>G MANE Select	NP_065690.2:p.Leu144=