Canonical Allele Identifier: CA260966089
Gene: FERMT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52933911T>C , CM000676.2:g.52933911T>C GRCh38
NC_000014.8:g.53400629T>C , CM000676.1:g.53400629T>C GRCh37
NC_000014.7:g.52470379T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341590.8:c.158-14555A>G MANE Select ENSP00000340391.3:n.158-14555A>G
ENST00000341590.7:c.158-14555A>G ENSP00000340391.3:n.158-14555A>G
ENST00000343279.8:c.158-14555A>G ENSP00000342858.4:n.158-14555A>G
ENST00000395631.6:c.158-14555A>G ENSP00000378993.2:n.158-14555A>G
ENST00000399304.7:c.158-14555A>G ENSP00000382243.3:n.158-14555A>G
ENST00000553373.5:c.158-14555A>G ENSP00000451084.1:n.158-14555A>G
ENST00000554712.5:c.158-14555A>G ENSP00000450506.1:n.158-14555A>G
ENST00000557562.1:c.177-14555A>G ENSP00000451085.1:n.177-14555A>G
NM_001134999.1:c.158-14555A>G NP_001128471.1:n.158-14555A>G
NM_001135000.1:c.158-14555A>G NP_001128472.1:n.158-14555A>G
NM_006832.2:c.158-14555A>G NP_006823.1:n.158-14555A>G
XM_005267285.1:c.158-14555A>G XP_005267342.1:n.158-14555A>G
XM_006720008.1:c.158-14555A>G XP_006720071.1:n.158-14555A>G
XM_006720009.1:c.158-14555A>G XP_006720072.1:n.158-14555A>G
XM_006720010.1:c.158-14555A>G XP_006720073.1:n.158-14555A>G
XM_005267285.3:c.158-14555A>G XP_005267342.1:n.158-14555A>G
XM_006720008.3:c.158-14555A>G XP_006720071.1:n.158-14555A>G
XM_006720009.3:c.158-14555A>G XP_006720072.1:n.158-14555A>G
XM_006720010.3:c.158-14555A>G XP_006720073.1:n.158-14555A>G
NM_006832.3:c.158-14555A>G MANE Select NP_006823.1:n.158-14555A>G
NM_001135000.2:c.158-14555A>G NP_001128472.1:n.158-14555A>G
NM_001134999.2:c.158-14555A>G NP_001128471.1:n.158-14555A>G
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