Canonical Allele Identifier: CA2751317155

Gene: SNRNP200

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.96293169_96293170insAG , CM000664.2:g.96293169_96293170insAG	GRCh38
NC_000002.11:g.96958907_96958908insAG , CM000664.1:g.96958907_96958908insAG	GRCh37
NC_000002.10:g.96322634_96322635insAG	NCBI36
NG_016973.1:g.17390_17391insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323853.10:c.2037-75_2037-74insCT MANE Select	ENSP00000317123.5:n.2037-75_2037-74insCT
ENST00000652267.1:c.2037-75_2037-74insCT	ENSP00000498933.1:n.2037-75_2037-74insCT
ENST00000323853.9:c.2037-75_2037-74insCT	ENSP00000317123.5:n.2037-75_2037-74insCT
NM_014014.4:c.2037-75_2037-74insCT	NP_054733.2:n.2037-75_2037-74insCT
NM_014014.5:c.2037-75_2037-74insCT MANE Select	NP_054733.2:n.2037-75_2037-74insCT