Canonical Allele Identifier: CA2790639604
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188619del , CM000673.2:g.19188619del GRCh38
NC_000011.9:g.19210166del , CM000673.1:g.19210166del GRCh37
NC_000011.8:g.19166742del NCBI36
NG_011932.2:g.26955del , LRG_440:g.26955del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-315del MANE Select ENSP00000265968.3:n.113-315del
ENST00000533783.2:c.113-315del ENSP00000431813.1:n.113-315del
ENST00000647990.1:c.113-315del ENSP00000496798.1:n.113-315del
ENST00000648719.1:c.113-3574del ENSP00000497633.1:n.113-3574del
ENST00000649235.1:c.113-315del ENSP00000497388.1:n.113-315del
ENST00000649842.1:c.113-2271del ENSP00000497531.1:n.113-2271del
ENST00000265968.7:c.113-315del ENSP00000265968.3:n.113-315del
ENST00000533783.1:c.113-315del ENSP00000431813.1:n.113-315del
NM_003476.4:c.113-315del NP_003467.1:n.113-315del
XM_024448698.1:c.113-2271del XP_024304466.1:n.113-2271del
NM_001369404.1:c.113-2271del NP_001356333.1:n.113-2271del
NM_003476.5:c.113-315del MANE Select NP_003467.1:n.113-315del