Canonical Allele Identifier: CA372062693

Gene: TRPS1

Linked Data

• dbSNP Id: rs1454331129
• gnomAD v3: 8-115414445-C-T
• gnomAD v4: 8-115414445-C-T
• MyVariant Identifiers: chr8:g.116426673C>T (hg19) ; chr8:g.115414445C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115414445C>T , CM000670.2:g.115414445C>T	GRCh38
NC_000008.10:g.116426673C>T , CM000670.1:g.116426673C>T	GRCh37
NC_000008.9:g.116495849C>T	NCBI36
NG_012383.3:g.259557G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.3463G>A MANE Select	ENSP00000379065.3:p.Val1155Met
ENST00000640765.1:c.3424G>A	ENSP00000492037.1:p.Val1142Met
ENST00000220888.9:c.3424G>A	ENSP00000220888.5:p.Val1142Met
ENST00000395715.7:c.3463G>A	ENSP00000379065.3:p.Val1155Met
ENST00000518018.1:c.797G>A
ENST00000519076.5:c.2686G>A	ENSP00000428910.1:p.Val896Met
ENST00000520276.5:c.3436G>A	ENSP00000428680.1:p.Val1146Met
NM_001282902.2:c.3436G>A	NP_001269831.1:p.Val1146Met
NM_001282903.2:c.3442G>A	NP_001269832.1:p.Val1148Met
NM_014112.4:c.3463G>A	NP_054831.2:p.Val1155Met
XM_005251049.2:c.3424G>A	XP_005251106.1:p.Val1142Met
XM_006716625.1:c.3463G>A	XP_006716688.1:p.Val1155Met
XM_011517264.1:c.3463G>A	XP_011515566.1:p.Val1155Met
XM_011517265.1:c.3463G>A	XP_011515567.1:p.Val1155Met
XM_011517266.1:c.3463G>A	XP_011515568.1:p.Val1155Met
XM_011517267.1:c.3442G>A	XP_011515569.1:p.Val1148Met
XM_011517268.1:c.3424G>A	XP_011515570.1:p.Val1142Met
NM_001330599.1:c.3424G>A	NP_001317528.1:p.Val1142Met
XM_011517264.2:c.3463G>A	XP_011515566.1:p.Val1155Met
XM_011517266.3:c.3463G>A	XP_011515568.1:p.Val1155Met
XM_011517268.2:c.3424G>A	XP_011515570.1:p.Val1142Met
NM_001282902.3:c.3436G>A	NP_001269831.1:p.Val1146Met
NM_001282903.3:c.3442G>A	NP_001269832.1:p.Val1148Met
NM_001330599.2:c.3424G>A	NP_001317528.1:p.Val1142Met
NM_014112.5:c.3463G>A MANE Select	NP_054831.2:p.Val1155Met