Canonical Allele Identifier: CA2573142809

Gene: TRPS1

Linked Data

• ClinVar Variation Id: 1620913
• ClinVar RCV Id: RCV002099337
• dbSNP Id: rs2129768290

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115418311del , CM000670.2:g.115418311del	GRCh38
NC_000008.10:g.116430539del , CM000670.1:g.116430539del	GRCh37
NC_000008.9:g.116499715del	NCBI36
NG_012383.3:g.255691del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.2823+19del MANE Select	ENSP00000379065.3:n.2823+19del
ENST00000640765.1:c.2784+19del	ENSP00000492037.1:n.2784+19del
ENST00000220888.9:c.2784+19del	ENSP00000220888.5:n.2784+19del
ENST00000395715.7:c.2823+19del	ENSP00000379065.3:n.2823+19del
ENST00000518018.1:c.157+19del
ENST00000519076.5:c.2046+19del	ENSP00000428910.1:n.2046+19del
ENST00000520276.5:c.2796+19del	ENSP00000428680.1:n.2796+19del
NM_001282902.2:c.2796+19del	NP_001269831.1:n.2796+19del
NM_001282903.2:c.2802+19del	NP_001269832.1:n.2802+19del
NM_014112.4:c.2823+19del	NP_054831.2:n.2823+19del
XM_005251049.2:c.2784+19del	XP_005251106.1:n.2784+19del
XM_006716625.1:c.2823+19del	XP_006716688.1:n.2823+19del
XM_011517264.1:c.2823+19del	XP_011515566.1:n.2823+19del
XM_011517265.1:c.2823+19del	XP_011515567.1:n.2823+19del
XM_011517266.1:c.2823+19del	XP_011515568.1:n.2823+19del
XM_011517267.1:c.2802+19del	XP_011515569.1:n.2802+19del
XM_011517268.1:c.2784+19del	XP_011515570.1:n.2784+19del
NM_001330599.1:c.2784+19del	NP_001317528.1:n.2784+19del
XM_011517264.2:c.2823+19del	XP_011515566.1:n.2823+19del
XM_011517266.3:c.2823+19del	XP_011515568.1:n.2823+19del
XM_011517268.2:c.2784+19del	XP_011515570.1:n.2784+19del
NM_001282902.3:c.2796+19del	NP_001269831.1:n.2796+19del
NM_001282903.3:c.2802+19del	NP_001269832.1:n.2802+19del
NM_001330599.2:c.2784+19del	NP_001317528.1:n.2784+19del
NM_014112.5:c.2823+19del MANE Select	NP_054831.2:n.2823+19del