Canonical Allele Identifier: CA379888152

Gene: CSRP3

Linked Data

• MyVariant Identifiers: chr11:g.19209703A>T (hg19) ; chr11:g.19188156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188156A>T , CM000673.2:g.19188156A>T	GRCh38
NC_000011.9:g.19209703A>T , CM000673.1:g.19209703A>T	GRCh37
NC_000011.8:g.19166279A>T	NCBI36
NG_011932.2:g.27418T>A , LRG_440:g.27418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.261T>A MANE Select	ENSP00000265968.3:p.His87Gln
ENST00000533783.2:c.261T>A	ENSP00000431813.1:p.His87Gln
ENST00000647990.1:c.261T>A	ENSP00000496798.1:p.His87Gln
ENST00000648719.1:c.113-3111T>A	ENSP00000497633.1:n.113-3111T>A
ENST00000649235.1:c.261T>A	ENSP00000497388.1:p.His87Gln
ENST00000649842.1:c.113-1808T>A	ENSP00000497531.1:n.113-1808T>A
ENST00000265968.7:c.261T>A	ENSP00000265968.3:p.His87Gln
ENST00000533783.1:c.261T>A	ENSP00000431813.1:p.His87Gln
NM_003476.4:c.261T>A	NP_003467.1:p.His87Gln
XM_024448698.1:c.113-1808T>A	XP_024304466.1:n.113-1808T>A
NM_001369404.1:c.113-1808T>A	NP_001356333.1:n.113-1808T>A
NM_003476.5:c.261T>A MANE Select	NP_003467.1:p.His87Gln