Canonical Allele Identifier: CA1240008123

Gene: DPYSL5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26860401T= , CM000664.2:g.26860401T=	GRCh38
NC_000002.11:g.27083269T= , CM000664.1:g.27083269T=	GRCh37
NC_000002.10:g.26936773T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000288699.11:c.-5+12147T= MANE Select	ENSP00000288699.6:n.-5+12147T=
ENST00000288699.10:c.-5+12147T=	ENSP00000288699.6:n.-5+12147T=
ENST00000401478.5:c.-5+12042T=	ENSP00000385549.1:n.-5+12042T=
ENST00000431402.5:c.-5+11904T=	ENSP00000399581.1:n.-5+11904T=
ENST00000434719.1:c.-5+11862T=	ENSP00000413075.1:n.-5+11862T=
ENST00000450961.5:c.-5+12534T=	ENSP00000407174.1:n.-5+12534T=
ENST00000614712.4:c.-5+11904T=	ENSP00000481305.1:n.-5+11904T=
NM_001253723.1:c.-5+12042T=	NP_001240652.1:n.-5+12042T=
NM_001253724.1:c.-5+11904T=	NP_001240653.1:n.-5+11904T=
NM_020134.3:c.-5+12147T=	NP_064519.2:n.-5+12147T=
XM_024453007.1:c.-5+10901T=	XP_024308775.1:n.-5+10901T=
XR_001738852.2:n.153+12147T=
NM_020134.4:c.-5+12147T= MANE Select	NP_064519.2:n.-5+12147T=
NM_001253723.2:c.-5+12042T=	NP_001240652.1:n.-5+12042T=
NM_001253724.2:c.-5+11904T=	NP_001240653.1:n.-5+11904T=