Canonical Allele Identifier: CA260959496
Gene: FERMT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52905612T>G , CM000676.2:g.52905612T>G GRCh38
NC_000014.8:g.53372330T>G , CM000676.1:g.53372330T>G GRCh37
NC_000014.7:g.52442080T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000341590.8:c.392-12185A>C MANE Select ENSP00000340391.3:n.392-12185A>C
ENST00000341590.7:c.392-12185A>C ENSP00000340391.3:n.392-12185A>C
ENST00000343279.8:c.392-12185A>C ENSP00000342858.4:n.392-12185A>C
ENST00000395631.6:c.392-12185A>C ENSP00000378993.2:n.392-12185A>C
ENST00000399304.7:c.392-12185A>C ENSP00000382243.3:n.392-12185A>C
ENST00000553373.5:c.392-12185A>C ENSP00000451084.1:n.392-12185A>C
ENST00000554152.5:c.218-12185A>C ENSP00000450741.1:n.218-12185A>C
ENST00000554288.1:c.77-12185A>C ENSP00000451268.1:n.77-12185A>C
ENST00000554712.5:c.392-12185A>C ENSP00000450506.1:n.392-12185A>C
ENST00000555692.5:c.260-12185A>C ENSP00000452472.1:n.260-12185A>C
ENST00000557562.1:c.*213-12185A>C ENSP00000451085.1:n.*213-12185A>C
NM_001134999.1:c.392-12185A>C NP_001128471.1:n.392-12185A>C
NM_001135000.1:c.392-12185A>C NP_001128472.1:n.392-12185A>C
NM_006832.2:c.392-12185A>C NP_006823.1:n.392-12185A>C
XM_005267285.1:c.392-12185A>C XP_005267342.1:n.392-12185A>C
XM_006720008.1:c.392-12185A>C XP_006720071.1:n.392-12185A>C
XM_006720009.1:c.392-12185A>C XP_006720072.1:n.392-12185A>C
XM_006720010.1:c.392-12185A>C XP_006720073.1:n.392-12185A>C
XR_943867.1:n.606+7458T>G
XR_943868.1:n.480+7458T>G
XM_005267285.3:c.392-12185A>C XP_005267342.1:n.392-12185A>C
XM_006720008.3:c.392-12185A>C XP_006720071.1:n.392-12185A>C
XM_006720009.3:c.392-12185A>C XP_006720072.1:n.392-12185A>C
XM_006720010.3:c.392-12185A>C XP_006720073.1:n.392-12185A>C
XR_943867.2:n.632+7458T>G
NM_006832.3:c.392-12185A>C MANE Select NP_006823.1:n.392-12185A>C
NM_001135000.2:c.392-12185A>C NP_001128472.1:n.392-12185A>C
NM_001134999.2:c.392-12185A>C NP_001128471.1:n.392-12185A>C
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