Canonical Allele Identifier: CA509455405
Gene: FERMT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.6060101T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.6079454T>A , CM000682.2:g.6079454T>A GRCh38
NC_000020.10:g.6060101T>A , CM000682.1:g.6060101T>A GRCh37
NC_000020.9:g.6008101T>A NCBI36
NG_016213.1:g.49091A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000699095.1:c.1842A>T ENSP00000514127.1:p.Val614=
ENST00000217289.9:c.1842A>T MANE Select ENSP00000217289.4:p.Val614=
ENST00000217289.8:c.1842A>T ENSP00000217289.4:p.Val614=
ENST00000478194.1:n.802A>T
ENST00000536936.1:c.1071A>T ENSP00000441063.1:p.Val357=
NM_017671.4:c.1842A>T NP_060141.3:p.Val614=
XM_024451935.1:c.1842A>T XP_024307703.1:p.Val614=
NM_017671.5:c.1842A>T MANE Select NP_060141.3:p.Val614=