Canonical Allele Identifier: CA14407203

Gene: MSI2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.57670055G>A , CM000679.2:g.57670055G>A	GRCh38
NC_000017.10:g.55747416G>A , CM000679.1:g.55747416G>A	GRCh37
NC_000017.9:g.53102415G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284073.7:c.791-4917G>A MANE Select	ENSP00000284073.2:n.791-4917G>A
ENST00000674964.1:c.791-4917G>A	ENSP00000502137.1:n.791-4917G>A
ENST00000675127.1:c.114-4917G>A
ENST00000675379.1:c.64-9494G>A
ENST00000675656.1:c.776-4863G>A	ENSP00000501595.1:n.776-4863G>A
ENST00000284073.6:c.791-4917G>A	ENSP00000284073.2:n.791-4917G>A
ENST00000416426.6:c.725-4863G>A	ENSP00000414671.2:n.725-4863G>A
ENST00000442934.6:c.608-4917G>A	ENSP00000392607.2:n.608-4917G>A
ENST00000579505.5:n.436-4863G>A
NM_138962.2:c.791-4917G>A	NP_620412.1:n.791-4917G>A
XM_005257014.2:c.791-4863G>A	XP_005257071.1:n.791-4863G>A
XM_005257015.2:c.791-4863G>A	XP_005257072.1:n.791-4863G>A
XM_011524284.1:c.790+17894G>A	XP_011522586.1:n.790+17894G>A
XM_011524286.1:c.479-4863G>A	XP_011522588.1:n.479-4863G>A
XM_011524287.1:c.443-4863G>A	XP_011522589.1:n.443-4863G>A
NM_001322250.1:c.725-4863G>A	NP_001309179.1:n.725-4863G>A
NM_138962.3:c.791-4917G>A	NP_620412.1:n.791-4917G>A
XM_005257014.3:c.791-4863G>A	XP_005257071.1:n.791-4863G>A
XM_005257015.3:c.791-4863G>A	XP_005257072.1:n.791-4863G>A
XM_011524286.2:c.479-4863G>A	XP_011522588.1:n.479-4863G>A
XM_011524287.3:c.443-4863G>A	XP_011522589.1:n.443-4863G>A
XM_017024147.2:c.698-4863G>A	XP_016879636.1:n.698-4863G>A
XM_017024149.2:c.530-4863G>A	XP_016879638.1:n.530-4863G>A
NM_138962.4:c.791-4917G>A MANE Select	NP_620412.1:n.791-4917G>A
NM_001322250.2:c.725-4863G>A	NP_001309179.1:n.725-4863G>A