Canonical Allele Identifier: CA420983451
Gene: EFNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.155106249T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155133773T>A , CM000663.2:g.155133773T>A GRCh38
NC_000001.10:g.155106249T>A , CM000663.1:g.155106249T>A GRCh37
NC_000001.9:g.153372873T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368407.8:c.498T>A MANE Select ENSP00000357392.3:p.Leu166=
ENST00000368406.2:c.432T>A ENSP00000357391.2:p.Leu144=
ENST00000368407.7:c.498T>A ENSP00000357392.3:p.Leu166=
ENST00000469878.5:n.749T>A
ENST00000474413.5:n.723T>A
ENST00000497282.1:n.541T>A
NM_004428.2:c.498T>A NP_004419.2:p.Leu166=
NM_182685.1:c.432T>A NP_872626.1:p.Leu144=
XM_005244940.3:c.309T>A XP_005244997.1:p.Leu103=
NM_004428.3:c.498T>A MANE Select NP_004419.2:p.Leu166=
NM_182685.2:c.432T>A NP_872626.1:p.Leu144=