Canonical Allele Identifier: CA2576810152
Gene: CEACAM16 HGNC NCBI
CEACAM16-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44704018_44704020del , CM000681.2:g.44704018_44704020del GRCh38
NC_000019.9:g.45207288_45207290del , CM000681.1:g.45207288_45207290del GRCh37
NC_000019.8:g.49899128_49899130del NCBI36
NG_032692.2:g.9868_9870del

Transcript Alleles

HGVS Amino-acid Change
ENST00000587331.7:c.383_385del (CEACAM16) MANE Select ENSP00000466561.1:p.Glu128_Ile129delinsVal
ENST00000405314.2:c.383_385del (CEACAM16) ENSP00000385576.1:p.Glu128_Ile129delinsVal
ENST00000587331.5:c.383_385del (CEACAM16) ENSP00000466561.1:p.Glu128_Ile129delinsVal
NM_001039213.3:c.383_385del (CEACAM16) NP_001034302.2:p.Glu128_Ile129delinsVal
XM_011526951.1:c.383_385del (CEACAM16) XP_011525253.1:p.Glu128_Ile129delinsVal
NM_001039213.4:c.383_385del (CEACAM16) MANE Select NP_001034302.2:p.Glu128_Ile129delinsVal
XM_017026795.1:c.383_385del (CEACAM16) XP_016882284.1:p.Glu128_Ile129delinsVal
XR_001753953.1:n.436-4843_436-4841del (CEACAM16-AS1)
XR_001753954.1:n.373-4843_373-4841del (CEACAM16-AS1)