Canonical Allele Identifier: CA1441689165
Gene: FAM184B HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.17681019_17681020delinsAC , CM000666.2:g.17681019_17681020delinsAC GRCh38
NC_000004.11:g.17682642_17682643delinsAC , CM000666.1:g.17682642_17682643delinsAC GRCh37
NC_000004.10:g.17291740_17291741delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000265018.4:c.1596+7404_1596+7405delinsGT MANE Select ENSP00000265018.3:n.1596+7404_1596+7405delinsGT
ENST00000265018.3:c.1596+7404_1596+7405delinsGT ENSP00000265018.3:n.1596+7404_1596+7405delinsGT
NM_015688.1:c.1596+7404_1596+7405delinsGT NP_056503.1:n.1596+7404_1596+7405delinsGT
XM_011513834.1:c.1596+7404_1596+7405delinsGT XP_011512136.1:n.1596+7404_1596+7405delinsGT
NM_015688.2:c.1596+7404_1596+7405delinsGT MANE Select NP_056503.1:n.1596+7404_1596+7405delinsGT
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