Canonical Allele Identifier: CA1611670044
Community Standard Title: NM_004233.4(CD83):c.489+606T=
Gene: CD83 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.14134361T= , CM000668.2:g.14134361T= GRCh38
NC_000006.11:g.14134592T= , CM000668.1:g.14134592T= GRCh37
NC_000006.10:g.14242571T= NCBI36
NG_030372.1:g.22106T=

Transcript Alleles

HGVS Amino-acid Change
NM_004233.4:c.489+606T= MANE Select NP_004224.1:n.489+606T=
ENST00000379153.4:c.489+606T= MANE Select ENSP00000368450.3:n.489+606T=
NM_001040280.1:c.489+606T= NP_001035370.1:n.489+606T=
NM_001040280.2:c.489+606T= NP_001035370.1:n.489+606T=
NM_001040280.3:c.489+606T= NP_001035370.1:n.489+606T=
NM_001251901.1:c.312+606T= NP_001238830.1:n.312+606T=
NM_004233.3:c.489+606T= NP_004224.1:n.489+606T=
ENST00000379153.3:c.489+606T= ENSP00000368450.3:n.489+606T=
ENST00000612003.4:c.312+606T= ENSP00000480760.1:n.312+606T=