Canonical Allele Identifier: CA1763170550

Gene: MSRA

Linked Data

• dbSNP Id: rs1800267345

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10292090C>T , CM000670.2:g.10292090C>T	GRCh38
NC_000008.10:g.10149600C>T , CM000670.1:g.10149600C>T	GRCh37
NC_000008.9:g.10187010C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000317173.9:c.332-9444C>T MANE Select	ENSP00000313921.4:n.332-9444C>T
ENST00000317173.8:c.332-9444C>T	ENSP00000313921.4:n.332-9444C>T
ENST00000382490.9:c.203-9444C>T	ENSP00000371930.5:n.203-9444C>T
ENST00000441698.6:c.212-9444C>T	ENSP00000410912.2:n.212-9444C>T
ENST00000518255.5:c.332-9444C>T	ENSP00000429461.1:n.332-9444C>T
ENST00000522907.5:c.134-9444C>T	ENSP00000428214.1:n.134-9444C>T
ENST00000523637.2:n.507-9444C>T
ENST00000528246.5:c.134-9444C>T	ENSP00000436839.1:n.134-9444C>T
NM_001135670.2:c.212-9444C>T	NP_001129142.1:n.212-9444C>T
NM_001135671.2:c.203-9444C>T	NP_001129143.1:n.203-9444C>T
NM_001199729.2:c.134-9444C>T	NP_001186658.1:n.134-9444C>T
NM_012331.4:c.332-9444C>T	NP_036463.1:n.332-9444C>T
XM_011543822.1:c.332-9444C>T	XP_011542124.1:n.332-9444C>T
XM_011543823.1:c.332-9444C>T	XP_011542125.1:n.332-9444C>T
XM_011543822.2:c.332-9444C>T	XP_011542124.1:n.332-9444C>T
XM_011543823.2:c.332-9444C>T	XP_011542125.1:n.332-9444C>T
XM_017013448.2:c.332-27793C>T	XP_016868937.1:n.332-27793C>T
XM_017013449.2:c.134-9444C>T	XP_016868938.1:n.134-9444C>T
XM_017013450.2:c.134-9444C>T	XP_016868939.1:n.134-9444C>T
XM_017013451.2:c.203-9444C>T	XP_016868940.1:n.203-9444C>T
NM_012331.5:c.332-9444C>T MANE Select	NP_036463.1:n.332-9444C>T
NM_001135670.3:c.212-9444C>T	NP_001129142.1:n.212-9444C>T
NM_001135671.3:c.203-9444C>T	NP_001129143.1:n.203-9444C>T
NM_001199729.3:c.134-9444C>T	NP_001186658.1:n.134-9444C>T