Canonical Allele Identifier: CA346987451
Community Standard Title: NM_001201543.2(FAM161A):c.1095T>G (p.Tyr365Ter)
Gene: FAM161A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61839909A>C , CM000664.2:g.61839909A>C GRCh38
NC_000002.11:g.62067044A>C , CM000664.1:g.62067044A>C GRCh37
NC_000002.10:g.61920548A>C NCBI36
NG_028125.1:g.19235T>G

Transcript Alleles

HGVS Amino-acid Change
NM_001201543.2:c.1095T>G MANE Select NP_001188472.1:p.Tyr365Ter
ENST00000404929.6:c.1095T>G MANE Select ENSP00000385158.1:p.Tyr365Ter
NM_001201543.1:c.1095T>G NP_001188472.1:p.Tyr365Ter
NM_032180.2:c.1095T>G NP_115556.2:p.Tyr365Ter
NM_032180.3:c.1095T>G NP_115556.2:p.Tyr365Ter
NR_037710.1:n.1141T>G
NR_037710.2:n.1058T>G
ENST00000307507.3:c.*1105T>G ENSP00000303170.3:n.*1105T>G
ENST00000404929.5:c.1095T>G ENSP00000385158.1:p.Tyr365Ter
ENST00000405894.3:c.1095T>G ENSP00000385893.3:p.Tyr365Ter
ENST00000418113.5:c.1082T>G
ENST00000456262.5:c.*610T>G ENSP00000396105.1:n.*610T>G
XM_017005072.1:c.768T>G XP_016860561.1:p.Tyr256Ter
XM_017005073.1:c.525T>G XP_016860562.1:p.Tyr175Ter
XM_017005074.1:c.525T>G XP_016860563.1:p.Tyr175Ter
XR_001738972.2:n.1096T>G
XR_001738973.2:n.1096T>G
XR_001738974.2:n.1096T>G
XR_001738975.2:n.1096T>G
XR_001738976.1:n.1124T>G
XR_001738977.1:n.1124T>G
XR_939724.1:n.2456T>G