Canonical Allele Identifier: CA1812945196

Gene: TRPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115586953T= , CM000670.2:g.115586953T=	GRCh38
NC_000008.10:g.116599180T= , CM000670.1:g.116599180T=	GRCh37
NC_000008.9:g.116668355T=	NCBI36
NG_012383.3:g.87049A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395715.8:c.2700+48A= MANE Select	ENSP00000379065.3:n.2700+48A=
ENST00000640765.1:c.2661+48A=	ENSP00000492037.1:n.2661+48A=
ENST00000220888.9:c.2661+48A=	ENSP00000220888.5:n.2661+48A=
ENST00000395715.7:c.2700+48A=	ENSP00000379065.3:n.2700+48A=
ENST00000519076.5:c.1923+48A=	ENSP00000428910.1:n.1923+48A=
ENST00000519674.1:c.2661+48A=	ENSP00000429174.1:n.2661+48A=
ENST00000520276.5:c.2673+48A=	ENSP00000428680.1:n.2673+48A=
NM_001282902.2:c.2673+48A=	NP_001269831.1:n.2673+48A=
NM_001282903.2:c.2679+48A=	NP_001269832.1:n.2679+48A=
NM_014112.4:c.2700+48A=	NP_054831.2:n.2700+48A=
XM_005251049.2:c.2661+48A=	XP_005251106.1:n.2661+48A=
XM_006716625.1:c.2700+48A=	XP_006716688.1:n.2700+48A=
XM_011517264.1:c.2700+48A=	XP_011515566.1:n.2700+48A=
XM_011517265.1:c.2700+48A=	XP_011515567.1:n.2700+48A=
XM_011517266.1:c.2700+48A=	XP_011515568.1:n.2700+48A=
XM_011517267.1:c.2679+48A=	XP_011515569.1:n.2679+48A=
XM_011517268.1:c.2661+48A=	XP_011515570.1:n.2661+48A=
NM_001330599.1:c.2661+48A=	NP_001317528.1:n.2661+48A=
XM_011517264.2:c.2700+48A=	XP_011515566.1:n.2700+48A=
XM_011517266.3:c.2700+48A=	XP_011515568.1:n.2700+48A=
XM_011517268.2:c.2661+48A=	XP_011515570.1:n.2661+48A=
NM_001282902.3:c.2673+48A=	NP_001269831.1:n.2673+48A=
NM_001282903.3:c.2679+48A=	NP_001269832.1:n.2679+48A=
NM_001330599.2:c.2661+48A=	NP_001317528.1:n.2661+48A=
NM_014112.5:c.2700+48A= MANE Select	NP_054831.2:n.2700+48A=