Canonical Allele Identifier: CA2678360480

Gene: SNRPC

Linked Data

• gnomAD v4: 6-34762533-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.34762535_34762536del , CM000668.2:g.34762535_34762536del	GRCh38
NC_000006.11:g.34730312_34730313del , CM000668.1:g.34730312_34730313del	GRCh37
NC_000006.10:g.34838290_34838291del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000244520.10:c.52-60_52-59del MANE Select	ENSP00000244520.5:n.52-60_52-59del
ENST00000244520.9:c.52-60_52-59del	ENSP00000244520.5:n.52-60_52-59del
ENST00000374017.3:c.115-60_115-59del	ENSP00000363129.3:n.115-60_115-59del
ENST00000374018.5:c.-72-60_-72-59del	ENSP00000363130.1:n.-72-60_-72-59del
ENST00000474635.1:n.44-60_44-59del
NM_003093.2:c.52-60_52-59del	NP_003084.1:n.52-60_52-59del
NR_029472.1:n.459-60_459-59del
NM_003093.3:c.52-60_52-59del MANE Select	NP_003084.1:n.52-60_52-59del
NR_029472.2:n.48-60_48-59del