Canonical Allele Identifier: CA12751894
Gene: MSRA HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10903323

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.10292057A>G , CM000670.2:g.10292057A>G GRCh38
NC_000008.9:g.10186977A>G NCBI36
NC_000008.10:g.10149567A>G , CM000670.1:g.10149567A>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000317173.8:c.332-9477A>G ENSP00000313921.4:p.=
ENST00000382490.9:c.203-9477A>G ENSP00000371930.5:p.=
ENST00000441698.6:c.212-9477A>G ENSP00000410912.2:p.=
ENST00000518255.5:c.332-9477A>G ENSP00000429461.1:p.=
ENST00000522907.5:c.134-9477A>G ENSP00000428214.1:p.=
ENST00000523637.2:n.507-9477A>G
ENST00000528246.5:c.134-9477A>G ENSP00000436839.1:p.=
NM_001135670.2:c.212-9477A>G VV NP_001129142.1:p.=
NM_001135671.2:c.203-9477A>G VV NP_001129143.1:p.=
NM_001199729.2:c.134-9477A>G VV NP_001186658.1:p.=
NM_012331.4:c.332-9477A>G VV NP_036463.1:p.=
XM_011543822.1:c.332-9477A>G XP_011542124.1:p.=
XM_011543823.1:c.332-9477A>G XP_011542125.1:p.=