Canonical Allele Identifier: CA1570861613
Gene: EFNA5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107646666A= , CM000667.2:g.107646666A= GRCh38
NC_000005.9:g.106982367A= , CM000667.1:g.106982367A= GRCh37
NC_000005.8:g.107010266A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000333274.11:c.125+23823T= MANE Select ENSP00000328777.6:n.125+23823T=
ENST00000333274.10:c.125+23823T= ENSP00000328777.6:n.125+23823T=
ENST00000504941.1:n.397+23823T=
ENST00000509503.1:c.125+23823T= ENSP00000426989.1:n.125+23823T=
NM_001962.2:c.125+23823T= NP_001953.1:n.125+23823T=
XM_006714565.1:c.125+23823T= XP_006714628.1:n.125+23823T=
XM_006714565.3:c.125+23823T= XP_006714628.1:n.125+23823T=
NM_001962.3:c.125+23823T= MANE Select NP_001953.1:n.125+23823T=
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