Canonical Allele Identifier: CA2173255693

Gene: STRC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.43616480G= , CM000677.2:g.43616480G=	GRCh38
NC_000015.9:g.43908678G= , CM000677.1:g.43908678G=	GRCh37
NC_000015.8:g.41695970G=	NCBI36
NG_011636.1:g.7321C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450892.7:c.1086C= MANE Select	ENSP00000401513.2:p.Tyr362=
ENST00000643290.1:c.1379+32C=	ENSP00000495476.1:n.1379+32C=
ENST00000428650.5:c.1086C=	ENSP00000415991.1:p.Tyr362=
ENST00000432436.1:c.906C=	ENSP00000407303.1:p.Tyr302=
ENST00000440125.5:c.1054+32C=	ENSP00000394866.1:n.1054+32C=
ENST00000450892.6:c.1086C=	ENSP00000401513.2:p.Tyr362=
ENST00000541030.5:c.-1024C=	ENSP00000440413.1:n.-1024C=
NM_153700.2:c.1086C= MANE Select	NP_714544.1:p.Tyr362=
XM_011521277.1:c.1575C=	XP_011519579.1:p.Tyr525=
XM_011521278.1:c.1113C=	XP_011519580.1:p.Tyr371=
XM_011521279.1:c.1113C=	XP_011519581.1:p.Tyr371=