Canonical Allele Identifier: CA1570740454
Gene: EFNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107388887C= , CM000667.2:g.107388887C= GRCh38
NC_000005.9:g.106724588C= , CM000667.1:g.106724588C= GRCh37
NC_000005.8:g.106752487C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000333274.11:c.419-1116G= MANE Select ENSP00000328777.6:n.419-1116G=
ENST00000333274.10:c.419-1116G= ENSP00000328777.6:n.419-1116G=
ENST00000509503.1:c.419-1116G= ENSP00000426989.1:n.419-1116G=
ENST00000611503.4:c.299-1116G= ENSP00000484681.1:n.299-1116G=
NM_001962.2:c.419-1116G= NP_001953.1:n.419-1116G=
XM_006714565.1:c.419-1116G= XP_006714628.1:n.419-1116G=
XM_011543250.1:c.365-1116G= XP_011541552.1:n.365-1116G=
XM_011543251.1:c.179-1116G= XP_011541553.1:n.179-1116G=
XM_006714565.3:c.419-1116G= XP_006714628.1:n.419-1116G=
XM_011543250.3:c.365-1116G= XP_011541552.1:n.365-1116G=
XM_011543251.2:c.179-1116G= XP_011541553.1:n.179-1116G=
XM_017009205.1:c.179-1116G= XP_016864694.1:n.179-1116G=
NM_001962.3:c.419-1116G= MANE Select NP_001953.1:n.419-1116G=