Canonical Allele Identifier: CA379888150

Gene: CSRP3

Linked Data

• MyVariant Identifiers: chr11:g.19209702G>T (hg19) ; chr11:g.19188155G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188155G>T , CM000673.2:g.19188155G>T	GRCh38
NC_000011.9:g.19209702G>T , CM000673.1:g.19209702G>T	GRCh37
NC_000011.8:g.19166278G>T	NCBI36
NG_011932.2:g.27419C>A , LRG_440:g.27419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.262C>A MANE Select	ENSP00000265968.3:p.Leu88Ile
ENST00000533783.2:c.262C>A	ENSP00000431813.1:p.Leu88Ile
ENST00000647990.1:c.262C>A	ENSP00000496798.1:p.Leu88Ile
ENST00000648719.1:c.113-3110C>A	ENSP00000497633.1:n.113-3110C>A
ENST00000649235.1:c.262C>A	ENSP00000497388.1:p.Leu88Ile
ENST00000649842.1:c.113-1807C>A	ENSP00000497531.1:n.113-1807C>A
ENST00000265968.7:c.262C>A	ENSP00000265968.3:p.Leu88Ile
ENST00000533783.1:c.262C>A	ENSP00000431813.1:p.Leu88Ile
NM_003476.4:c.262C>A	NP_003467.1:p.Leu88Ile
XM_024448698.1:c.113-1807C>A	XP_024304466.1:n.113-1807C>A
NM_001369404.1:c.113-1807C>A	NP_001356333.1:n.113-1807C>A
NM_003476.5:c.262C>A MANE Select	NP_003467.1:p.Leu88Ile