Canonical Allele Identifier: CA462658145

Gene: TRPS1

Linked Data

• MyVariant Identifiers: chr8:g.116426413C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115414185C>A , CM000670.2:g.115414185C>A	GRCh38
NC_000008.10:g.116426413C>A , CM000670.1:g.116426413C>A	GRCh37
NC_000008.9:g.116495589C>A	NCBI36
NG_012383.3:g.259817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.3723G>T MANE Select	ENSP00000379065.3:p.Val1241=
ENST00000640765.1:c.3684G>T	ENSP00000492037.1:p.Val1228=
ENST00000220888.9:c.3684G>T	ENSP00000220888.5:p.Val1228=
ENST00000395715.7:c.3723G>T	ENSP00000379065.3:p.Val1241=
ENST00000519076.5:c.2946G>T	ENSP00000428910.1:p.Val982=
ENST00000520276.5:c.3696G>T	ENSP00000428680.1:p.Val1232=
NM_001282902.2:c.3696G>T	NP_001269831.1:p.Val1232=
NM_001282903.2:c.3702G>T	NP_001269832.1:p.Val1234=
NM_014112.4:c.3723G>T	NP_054831.2:p.Val1241=
XM_005251049.2:c.3684G>T	XP_005251106.1:p.Val1228=
XM_006716625.1:c.3723G>T	XP_006716688.1:p.Val1241=
XM_011517264.1:c.3723G>T	XP_011515566.1:p.Val1241=
XM_011517265.1:c.3723G>T	XP_011515567.1:p.Val1241=
XM_011517266.1:c.3723G>T	XP_011515568.1:p.Val1241=
XM_011517267.1:c.3702G>T	XP_011515569.1:p.Val1234=
XM_011517268.1:c.3684G>T	XP_011515570.1:p.Val1228=
NM_001330599.1:c.3684G>T	NP_001317528.1:p.Val1228=
XM_011517264.2:c.3723G>T	XP_011515566.1:p.Val1241=
XM_011517266.3:c.3723G>T	XP_011515568.1:p.Val1241=
XM_011517268.2:c.3684G>T	XP_011515570.1:p.Val1228=
NM_001282902.3:c.3696G>T	NP_001269831.1:p.Val1232=
NM_001282903.3:c.3702G>T	NP_001269832.1:p.Val1234=
NM_001330599.2:c.3684G>T	NP_001317528.1:p.Val1228=
NM_014112.5:c.3723G>T MANE Select	NP_054831.2:p.Val1241=