Canonical Allele Identifier: CA844784198

Gene: MSRA

Linked Data

• dbSNP Id: rs1320009976
• gnomAD v3: 8-10291795-G-GA
• gnomAD v4: 8-10291795-G-GA
• MyVariant Identifiers: chr8:g.10149305_10149306insA (hg19) ; chr8:g.10291795_10291796insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.10291803dup , CM000670.2:g.10291803dup	GRCh38
NC_000008.10:g.10149313dup , CM000670.1:g.10149313dup	GRCh37
NC_000008.9:g.10186723dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317173.9:c.332-9731dup MANE Select	ENSP00000313921.4:n.332-9731dup
ENST00000317173.8:c.332-9731dup	ENSP00000313921.4:n.332-9731dup
ENST00000382490.9:c.203-9731dup	ENSP00000371930.5:n.203-9731dup
ENST00000441698.6:c.212-9731dup	ENSP00000410912.2:n.212-9731dup
ENST00000518255.5:c.332-9731dup	ENSP00000429461.1:n.332-9731dup
ENST00000522907.5:c.134-9731dup	ENSP00000428214.1:n.134-9731dup
ENST00000523637.2:n.507-9731dup
ENST00000528246.5:c.134-9731dup	ENSP00000436839.1:n.134-9731dup
NM_001135670.2:c.212-9731dup	NP_001129142.1:n.212-9731dup
NM_001135671.2:c.203-9731dup	NP_001129143.1:n.203-9731dup
NM_001199729.2:c.134-9731dup	NP_001186658.1:n.134-9731dup
NM_012331.4:c.332-9731dup	NP_036463.1:n.332-9731dup
XM_011543822.1:c.332-9731dup	XP_011542124.1:n.332-9731dup
XM_011543823.1:c.332-9731dup	XP_011542125.1:n.332-9731dup
XM_011543822.2:c.332-9731dup	XP_011542124.1:n.332-9731dup
XM_011543823.2:c.332-9731dup	XP_011542125.1:n.332-9731dup
XM_017013448.2:c.332-28080dup	XP_016868937.1:n.332-28080dup
XM_017013449.2:c.134-9731dup	XP_016868938.1:n.134-9731dup
XM_017013450.2:c.134-9731dup	XP_016868939.1:n.134-9731dup
XM_017013451.2:c.203-9731dup	XP_016868940.1:n.203-9731dup
NM_012331.5:c.332-9731dup MANE Select	NP_036463.1:n.332-9731dup
NM_001135670.3:c.212-9731dup	NP_001129142.1:n.212-9731dup
NM_001135671.3:c.203-9731dup	NP_001129143.1:n.203-9731dup
NM_001199729.3:c.134-9731dup	NP_001186658.1:n.134-9731dup