Canonical Allele Identifier: CA2497195724

Gene: PDE1C

Linked Data

• dbSNP Id: rs1809444506

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.32252197_32252200del , CM000669.2:g.32252197_32252200del	GRCh38
NC_000007.13:g.32291809_32291812del , CM000669.1:g.32291809_32291812del	GRCh37
NC_000007.12:g.32258334_32258337del	NCBI36
NG_051183.1:g.181028_181031del

Transcript Alleles

HGVS	Amino-acid change
ENST00000672256.1:c.311-42658_311-42655del	ENSP00000499831.1:n.311-42658_311-42655de...
ENST00000396193.5:c.86-42658_86-42655del	ENSP00000379496.1:n.86-42658_86-42655del
NM_001191058.2:c.86-42658_86-42655del	NP_001177987.2:n.86-42658_86-42655del
XM_005249768.3:c.86-42658_86-42655del	XP_005249825.2:n.86-42658_86-42655del
XM_011515410.1:c.86-42658_86-42655del	XP_011513712.1:n.86-42658_86-42655del
XM_011515411.1:c.86-42658_86-42655del	XP_011513713.1:n.86-42658_86-42655del
XM_011515414.1:c.86-42658_86-42655del	XP_011513716.1:n.86-42658_86-42655del
NM_001191058.3:c.86-42658_86-42655del	NP_001177987.2:n.86-42658_86-42655del
NM_001322058.1:c.86-42658_86-42655del	NP_001308987.1:n.86-42658_86-42655del
NM_001322059.1:c.311-42658_311-42655del	NP_001308988.1:n.311-42658_311-42655del
XM_017012264.1:c.190+41062_190+41065del	XP_016867753.1:n.190+41062_190+41065del
XM_017012265.1:c.25+6680_25+6683del	XP_016867754.1:n.25+6680_25+6683del
XM_017012266.1:c.190+41062_190+41065del	XP_016867755.1:n.190+41062_190+41065del
XR_001744802.1:n.205+41062_205+41065del
XR_001744803.1:n.205+41062_205+41065del
XR_001744804.1:n.205+41062_205+41065del
XR_001744805.1:n.205+41062_205+41065del
NM_001191058.4:c.86-42658_86-42655del	NP_001177987.2:n.86-42658_86-42655del
NM_001322058.2:c.86-42658_86-42655del	NP_001308987.1:n.86-42658_86-42655del
NM_001322059.2:c.311-42658_311-42655del	NP_001308988.1:n.311-42658_311-42655del