Canonical Allele Identifier: CA124716389
Gene: EFNA5 HGNC NCBI

Linked Data

dbSNP Id: rs375572073
MyVariant Identifiers: chr5:g.106982679G>A (hg19) chr5:g.107646978G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107646978G>A , CM000667.2:g.107646978G>A GRCh38
NC_000005.9:g.106982679G>A , CM000667.1:g.106982679G>A GRCh37
NC_000005.8:g.107010578G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000333274.11:c.125+23511C>T MANE Select ENSP00000328777.6:n.125+23511C>T
ENST00000333274.10:c.125+23511C>T ENSP00000328777.6:n.125+23511C>T
ENST00000504941.1:n.397+23511C>T
ENST00000509503.1:c.125+23511C>T ENSP00000426989.1:n.125+23511C>T
NM_001962.2:c.125+23511C>T NP_001953.1:n.125+23511C>T
XM_006714565.1:c.125+23511C>T XP_006714628.1:n.125+23511C>T
XM_006714565.3:c.125+23511C>T XP_006714628.1:n.125+23511C>T
NM_001962.3:c.125+23511C>T MANE Select NP_001953.1:n.125+23511C>T
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