Canonical Allele Identifier: CA372062765

Gene: TRPS1

Linked Data

• dbSNP Id: rs1180274964
• gnomAD v2: 8-116426706-C-T
• gnomAD v3: 8-115414478-C-T
• gnomAD v4: 8-115414478-C-T
• COSMIC: COSM3164436 ; COSM3164437
• MyVariant Identifiers: chr8:g.116426706C>T (hg19) ; chr8:g.115414478C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115414478C>T , CM000670.2:g.115414478C>T	GRCh38
NC_000008.10:g.116426706C>T , CM000670.1:g.116426706C>T	GRCh37
NC_000008.9:g.116495882C>T	NCBI36
NG_012383.3:g.259524G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.3430G>A MANE Select	ENSP00000379065.3:p.Val1144Met
ENST00000640765.1:c.3391G>A	ENSP00000492037.1:p.Val1131Met
ENST00000220888.9:c.3391G>A	ENSP00000220888.5:p.Val1131Met
ENST00000395715.7:c.3430G>A	ENSP00000379065.3:p.Val1144Met
ENST00000518018.1:c.764G>A
ENST00000519076.5:c.2653G>A	ENSP00000428910.1:p.Val885Met
ENST00000520276.5:c.3403G>A	ENSP00000428680.1:p.Val1135Met
NM_001282902.2:c.3403G>A	NP_001269831.1:p.Val1135Met
NM_001282903.2:c.3409G>A	NP_001269832.1:p.Val1137Met
NM_014112.4:c.3430G>A	NP_054831.2:p.Val1144Met
XM_005251049.2:c.3391G>A	XP_005251106.1:p.Val1131Met
XM_006716625.1:c.3430G>A	XP_006716688.1:p.Val1144Met
XM_011517264.1:c.3430G>A	XP_011515566.1:p.Val1144Met
XM_011517265.1:c.3430G>A	XP_011515567.1:p.Val1144Met
XM_011517266.1:c.3430G>A	XP_011515568.1:p.Val1144Met
XM_011517267.1:c.3409G>A	XP_011515569.1:p.Val1137Met
XM_011517268.1:c.3391G>A	XP_011515570.1:p.Val1131Met
NM_001330599.1:c.3391G>A	NP_001317528.1:p.Val1131Met
XM_011517264.2:c.3430G>A	XP_011515566.1:p.Val1144Met
XM_011517266.3:c.3430G>A	XP_011515568.1:p.Val1144Met
XM_011517268.2:c.3391G>A	XP_011515570.1:p.Val1131Met
NM_001282902.3:c.3403G>A	NP_001269831.1:p.Val1135Met
NM_001282903.3:c.3409G>A	NP_001269832.1:p.Val1137Met
NM_001330599.2:c.3391G>A	NP_001317528.1:p.Val1131Met
NM_014112.5:c.3430G>A MANE Select	NP_054831.2:p.Val1144Met