Canonical Allele Identifier: CA11004643

Gene: DPYSL5

Genomic Alleles

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

Transcript Alleles

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