Canonical Allele Identifier: CA1812945323

Gene: TRPS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.115587048C= , CM000670.2:g.115587048C=	GRCh38
NC_000008.10:g.116599275C= , CM000670.1:g.116599275C=	GRCh37
NC_000008.9:g.116668450C=	NCBI36
NG_012383.3:g.86954G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000395715.8:c.2653G= MANE Select	ENSP00000379065.3:p.Ala885=
ENST00000640765.1:c.2614G=	ENSP00000492037.1:p.Ala872=
ENST00000220888.9:c.2614G=	ENSP00000220888.5:p.Ala872=
ENST00000395715.7:c.2653G=	ENSP00000379065.3:p.Ala885=
ENST00000517323.2:c.2026G=	ENSP00000430803.2:p.Ala676=
ENST00000519076.5:c.1876G=	ENSP00000428910.1:p.Ala626=
ENST00000519674.1:c.2614G=	ENSP00000429174.1:p.Ala872=
ENST00000520276.5:c.2626G=	ENSP00000428680.1:p.Ala876=
NM_001282902.2:c.2626G=	NP_001269831.1:p.Ala876=
NM_001282903.2:c.2632G=	NP_001269832.1:p.Ala878=
NM_014112.4:c.2653G=	NP_054831.2:p.Ala885=
XM_005251049.2:c.2614G=	XP_005251106.1:p.Ala872=
XM_006716625.1:c.2653G=	XP_006716688.1:p.Ala885=
XM_011517264.1:c.2653G=	XP_011515566.1:p.Ala885=
XM_011517265.1:c.2653G=	XP_011515567.1:p.Ala885=
XM_011517266.1:c.2653G=	XP_011515568.1:p.Ala885=
XM_011517267.1:c.2632G=	XP_011515569.1:p.Ala878=
XM_011517268.1:c.2614G=	XP_011515570.1:p.Ala872=
NM_001330599.1:c.2614G=	NP_001317528.1:p.Ala872=
XM_011517264.2:c.2653G=	XP_011515566.1:p.Ala885=
XM_011517266.3:c.2653G=	XP_011515568.1:p.Ala885=
XM_011517268.2:c.2614G=	XP_011515570.1:p.Ala872=
NM_001282902.3:c.2626G=	NP_001269831.1:p.Ala876=
NM_001282903.3:c.2632G=	NP_001269832.1:p.Ala878=
NM_001330599.2:c.2614G=	NP_001317528.1:p.Ala872=
NM_014112.5:c.2653G= MANE Select	NP_054831.2:p.Ala885=