Canonical Allele Identifier: CA2243307022
Gene: SRR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2313019C= , CM000679.2:g.2313019C= GRCh38
NC_000017.10:g.2216313C= , CM000679.1:g.2216313C= GRCh37
NC_000017.9:g.2163063C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000344595.10:c.-4-2538C= MANE Select ENSP00000339435.5:n.-4-2538C=
ENST00000344595.9:c.-4-2538C= ENSP00000339435.5:n.-4-2538C=
ENST00000570662.2:c.-4-2538C= ENSP00000460581.2:n.-4-2538C=
ENST00000572709.5:c.-4-2538C= ENSP00000458814.1:n.-4-2538C=
ENST00000574987.1:c.-279-4851C= ENSP00000461343.1:n.-279-4851C=
ENST00000575840.5:c.-4-2538C= ENSP00000461589.1:n.-4-2538C=
ENST00000576620.5:c.-4-2538C= ENSP00000461125.1:n.-4-2538C=
ENST00000576848.1:c.-85+9002C= ENSP00000476682.1:n.-85+9002C=
NM_001304803.1:c.-279-4851C= NP_001291732.1:n.-279-4851C=
NM_021947.2:c.-4-2538C= NP_068766.1:n.-4-2538C=
XM_006721565.2:c.-4-2538C= XP_006721628.1:n.-4-2538C=
XM_006721566.2:c.-4-2538C= XP_006721629.1:n.-4-2538C=
XM_011523974.1:c.-4-2538C= XP_011522276.1:n.-4-2538C=
XM_011523975.1:c.-4-2538C= XP_011522277.1:n.-4-2538C=
XM_006721565.3:c.-4-2538C= XP_006721628.1:n.-4-2538C=
XM_006721566.3:c.-4-2538C= XP_006721629.1:n.-4-2538C=
XM_011523974.3:c.-4-2538C= XP_011522276.1:n.-4-2538C=
NM_021947.3:c.-4-2538C= MANE Select NP_068766.1:n.-4-2538C=