Canonical Allele Identifier: CA342648791

Gene: EFNA1

Linked Data

• MyVariant Identifiers: chr1:g.155106208C>A (hg19) ; chr1:g.155133732C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155133732C>A , CM000663.2:g.155133732C>A	GRCh38
NC_000001.10:g.155106208C>A , CM000663.1:g.155106208C>A	GRCh37
NC_000001.9:g.153372832C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368407.8:c.457C>A MANE Select	ENSP00000357392.3:p.His153Asn
ENST00000368406.2:c.391C>A	ENSP00000357391.2:p.His131Asn
ENST00000368407.7:c.457C>A	ENSP00000357392.3:p.His153Asn
ENST00000469878.5:n.708C>A
ENST00000474413.5:n.682C>A
ENST00000497282.1:n.500C>A
NM_004428.2:c.457C>A	NP_004419.2:p.His153Asn
NM_182685.1:c.391C>A	NP_872626.1:p.His131Asn
XM_005244940.3:c.268C>A	XP_005244997.1:p.His90Asn
NM_004428.3:c.457C>A MANE Select	NP_004419.2:p.His153Asn
NM_182685.2:c.391C>A	NP_872626.1:p.His131Asn