Canonical Allele Identifier: CA2243286636

Gene: SRR

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2304032G= , CM000679.2:g.2304032G=	GRCh38
NC_000017.10:g.2207326G= , CM000679.1:g.2207326G=	GRCh37
NC_000017.9:g.2154076G=	NCBI36
NG_033980.1:g.4744C=

Transcript Alleles

HGVS	Amino-acid Change
NM_021947.3:c.-5+15G= MANE Select	NP_068766.1:n.-5+15G=
ENST00000344595.10:c.-5+15G= MANE Select	ENSP00000339435.5:n.-5+15G=
NM_001304803.1:c.-280+15G=	NP_001291732.1:n.-280+15G=
NM_021947.2:c.-5+15G=	NP_068766.1:n.-5+15G=
ENST00000344595.9:c.-5+15G=	ENSP00000339435.5:n.-5+15G=
ENST00000572709.5:c.-5+555G=	ENSP00000458814.1:n.-5+555G=
ENST00000574987.1:c.-280+15G=	ENSP00000461343.1:n.-280+15G=
ENST00000575840.5:c.-219+15G=	ENSP00000461589.1:n.-219+15G=
ENST00000576620.5:c.-5+15G=	ENSP00000461125.1:n.-5+15G=
ENST00000576848.1:c.-85+15G=	ENSP00000476682.1:n.-85+15G=
XM_006721565.2:c.-5+555G=	XP_006721628.1:n.-5+555G=
XM_006721565.3:c.-5+555G=	XP_006721628.1:n.-5+555G=
XM_011523975.1:c.-5+15G=	XP_011522277.1:n.-5+15G=