Canonical Allele Identifier: CA420983433
Gene: EFNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.155106216T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.155133740T>A , CM000663.2:g.155133740T>A GRCh38
NC_000001.10:g.155106216T>A , CM000663.1:g.155106216T>A GRCh37
NC_000001.9:g.153372840T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000368407.8:c.465T>A MANE Select ENSP00000357392.3:p.Pro155=
ENST00000368406.2:c.399T>A ENSP00000357391.2:p.Pro133=
ENST00000368407.7:c.465T>A ENSP00000357392.3:p.Pro155=
ENST00000469878.5:n.716T>A
ENST00000474413.5:n.690T>A
ENST00000497282.1:n.508T>A
NM_004428.2:c.465T>A NP_004419.2:p.Pro155=
NM_182685.1:c.399T>A NP_872626.1:p.Pro133=
XM_005244940.3:c.276T>A XP_005244997.1:p.Pro92=
NM_004428.3:c.465T>A MANE Select NP_004419.2:p.Pro155=
NM_182685.2:c.399T>A NP_872626.1:p.Pro133=