Canonical Allele Identifier: CA15752476

Gene: NT5DC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103799046C>G , CM000674.2:g.103799046C>G	GRCh38
NC_000012.11:g.104192824C>G , CM000674.1:g.104192824C>G	GRCh37
NC_000012.10:g.102716954C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001031701.3:c.525-369G>C MANE Select	NP_001026871.1:n.525-369G>C
ENST00000392876.8:c.525-369G>C MANE Select	ENSP00000376615.3:n.525-369G>C
NM_001031701.2:c.525-369G>C	NP_001026871.1:n.525-369G>C
ENST00000392876.7:c.525-369G>C	ENSP00000376615.3:n.525-369G>C
ENST00000465502.1:n.323-369G>C
XM_011538476.1:c.84-369G>C	XP_011536778.1:n.84-369G>C
XM_011538476.2:c.84-369G>C	XP_011536778.1:n.84-369G>C
XM_017019454.1:c.525-369G>C	XP_016874943.1:n.525-369G>C
XR_001748756.1:n.581-369G>C
XR_001748757.1:n.593-369G>C
XR_001748758.1:n.593-369G>C
XR_001748759.1:n.600-369G>C
XR_001748760.2:n.608-369G>C
XR_944574.1:n.603-369G>C
XR_944574.2:n.581-369G>C
XR_944575.1:n.603-369G>C
XR_944576.1:n.603-369G>C
XR_944577.1:n.603-369G>C
XR_944578.1:n.603-369G>C
XR_944579.1:n.610-369G>C
XR_944580.1:n.610-369G>C
XR_944580.2:n.600-369G>C
XR_944581.1:n.610-369G>C
XR_944581.2:n.602-369G>C
XR_944582.1:n.610-369G>C
XR_944582.2:n.603-369G>C
XR_944583.1:n.614-369G>C