Canonical Allele Identifier: CA16468105
Gene: DLEU2 HGNC NCBI
SPRYD7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.49989311C>T , CM000675.2:g.49989311C>T GRCh38
NC_000013.10:g.50563447C>T , CM000675.1:g.50563447C>T GRCh37
NC_000013.9:g.49461448C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_002612.1:n.1530-690G>A (DLEU2)
XM_011535166.1:c.223-690G>A (SPRYD7) XP_011533468.1:n.223-690G>A
XM_011535167.1:c.223-690G>A (SPRYD7) XP_011533469.1:n.223-690G>A
NR_152566.1:n.1830-690G>A (DLEU2)