Canonical Allele Identifier: CA1570861734
Gene: EFNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107646961_107646963delinsCTG , CM000667.2:g.107646961_107646963delinsCTG GRCh38
NC_000005.9:g.106982662_106982664delinsCTG , CM000667.1:g.106982662_106982664delinsCTG GRCh37
NC_000005.8:g.107010561_107010563delinsCTG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000333274.11:c.125+23526_125+23528delinsCAG MANE Select ENSP00000328777.6:n.125+23526_125+23528delinsCAG
ENST00000333274.10:c.125+23526_125+23528delinsCAG ENSP00000328777.6:n.125+23526_125+23528delinsCAG
ENST00000504941.1:n.397+23526_397+23528delinsCAG
ENST00000509503.1:c.125+23526_125+23528delinsCAG ENSP00000426989.1:n.125+23526_125+23528delinsCAG
NM_001962.2:c.125+23526_125+23528delinsCAG NP_001953.1:n.125+23526_125+23528delinsCAG
XM_006714565.1:c.125+23526_125+23528delinsCAG XP_006714628.1:n.125+23526_125+23528delinsCAG
XM_006714565.3:c.125+23526_125+23528delinsCAG XP_006714628.1:n.125+23526_125+23528delinsCAG
NM_001962.3:c.125+23526_125+23528delinsCAG MANE Select NP_001953.1:n.125+23526_125+23528delinsCAG