Canonical Allele Identifier: CA365192951

Gene: CD164

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.109368301T>C , CM000668.2:g.109368301T>C	GRCh38
NC_000006.11:g.109689504T>C , CM000668.1:g.109689504T>C	GRCh37
NC_000006.10:g.109796197T>C	NCBI36
NG_051926.1:g.19512A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_006016.6:c.*550A>G MANE Select	NP_006007.2:n.*550A>G
ENST00000310786.10:c.*550A>G MANE Select	ENSP00000309376.4:n.*550A>G
NM_001142401.1:c.*550A>G	NP_001135873.1:n.*550A>G
NM_001142401.2:c.*550A>G	NP_001135873.1:n.*550A>G
NM_001142401.3:c.*550A>G	NP_001135873.1:n.*550A>G
NM_001142402.1:c.*550A>G	NP_001135874.1:n.*550A>G
NM_001142402.2:c.*550A>G	NP_001135874.1:n.*550A>G
NM_001142402.3:c.*550A>G	NP_001135874.1:n.*550A>G
NM_001142403.1:c.548A>G	NP_001135875.1:p.Tyr183Cys
NM_001142403.2:c.548A>G	NP_001135875.1:p.Tyr183Cys
NM_001142403.3:c.548A>G	NP_001135875.1:p.Tyr183Cys
NM_001142404.1:c.452A>G	NP_001135876.1:p.Tyr151Cys
NM_001142404.2:c.452A>G	NP_001135876.1:p.Tyr151Cys
NM_001142404.3:c.452A>G	NP_001135876.1:p.Tyr151Cys
NM_001346500.1:c.*550A>G	NP_001333429.1:n.*550A>G
NM_001346500.2:c.*550A>G	NP_001333429.1:n.*550A>G
NM_006016.4:c.*550A>G	NP_006007.2:n.*550A>G
NM_006016.5:c.*550A>G	NP_006007.2:n.*550A>G
ENST00000275080.11:c.*550A>G	ENSP00000275080.7:n.*550A>G
ENST00000310786.8:c.*550A>G	ENSP00000309376.4:n.*550A>G
ENST00000324953.9:c.*550A>G	ENSP00000314177.5:n.*550A>G
ENST00000368961.9:c.*696A>G	ENSP00000357957.6:n.*696A>G
ENST00000413644.6:c.548A>G	ENSP00000402237.2:p.Tyr183Cys
ENST00000415861.2:n.3176A>G
ENST00000499860.6:n.1823A>G
ENST00000504373.1:c.*550A>G	ENSP00000422999.1:n.*550A>G
ENST00000504373.2:c.*550A>G	ENSP00000422999.1:n.*550A>G
ENST00000512821.5:c.452A>G	ENSP00000427546.1:p.Tyr151Cys