Canonical Allele Identifier: CA1570861766
Gene: EFNA5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107647001_107647004delinsTAAC , CM000667.2:g.107647001_107647004delinsTAAC GRCh38
NC_000005.9:g.106982702_106982705delinsTAAC , CM000667.1:g.106982702_106982705delinsTAAC GRCh37
NC_000005.8:g.107010601_107010604delinsTAAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000333274.11:c.125+23485_125+23488delinsGTTA MANE Select ENSP00000328777.6:n.125+23485_125+23488delinsGTTA
ENST00000333274.10:c.125+23485_125+23488delinsGTTA ENSP00000328777.6:n.125+23485_125+23488delinsGTTA
ENST00000504941.1:n.397+23485_397+23488delinsGTTA
ENST00000509503.1:c.125+23485_125+23488delinsGTTA ENSP00000426989.1:n.125+23485_125+23488delinsGTTA
NM_001962.2:c.125+23485_125+23488delinsGTTA NP_001953.1:n.125+23485_125+23488delinsGTTA
XM_006714565.1:c.125+23485_125+23488delinsGTTA XP_006714628.1:n.125+23485_125+23488delinsGTTA
XM_006714565.3:c.125+23485_125+23488delinsGTTA XP_006714628.1:n.125+23485_125+23488delinsGTTA
NM_001962.3:c.125+23485_125+23488delinsGTTA MANE Select NP_001953.1:n.125+23485_125+23488delinsGTTA