Canonical Allele Identifier: CA2678360483

Gene: SNRPC

Linked Data

• gnomAD v4: 6-34762548-T-TTTA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762548_34762549insTTA , CM000668.2:g.34762548_34762549insTTA	GRCh38
NC_000006.11:g.34730325_34730326insTTA , CM000668.1:g.34730325_34730326insTTA	GRCh37
NC_000006.10:g.34838303_34838304insTTA	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.52-47_52-46insTTA MANE Select	ENSP00000244520.5:n.52-47_52-46insTTA
ENST00000244520.9:c.52-47_52-46insTTA	ENSP00000244520.5:n.52-47_52-46insTTA
ENST00000374017.3:c.115-47_115-46insTTA	ENSP00000363129.3:n.115-47_115-46insTTA
ENST00000374018.5:c.-72-47_-72-46insTTA	ENSP00000363130.1:n.-72-47_-72-46insTTA
ENST00000474635.1:n.44-47_44-46insTTA
NM_003093.2:c.52-47_52-46insTTA	NP_003084.1:n.52-47_52-46insTTA
NR_029472.1:n.459-47_459-46insTTA
NM_003093.3:c.52-47_52-46insTTA MANE Select	NP_003084.1:n.52-47_52-46insTTA
NR_029472.2:n.48-47_48-46insTTA