Canonical Allele Identifier: CA124716374

Gene: EFNA5

Linked Data

• dbSNP Id: rs982866358
• MyVariant Identifiers: chr5:g.106982480G>T (hg19) ; chr5:g.107646779G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.107646779G>T , CM000667.2:g.107646779G>T	GRCh38
NC_000005.9:g.106982480G>T , CM000667.1:g.106982480G>T	GRCh37
NC_000005.8:g.107010379G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000333274.11:c.125+23710C>A MANE Select	ENSP00000328777.6:n.125+23710C>A
ENST00000333274.10:c.125+23710C>A	ENSP00000328777.6:n.125+23710C>A
ENST00000504941.1:n.397+23710C>A
ENST00000509503.1:c.125+23710C>A	ENSP00000426989.1:n.125+23710C>A
NM_001962.2:c.125+23710C>A	NP_001953.1:n.125+23710C>A
XM_006714565.1:c.125+23710C>A	XP_006714628.1:n.125+23710C>A
XM_006714565.3:c.125+23710C>A	XP_006714628.1:n.125+23710C>A
NM_001962.3:c.125+23710C>A MANE Select	NP_001953.1:n.125+23710C>A