Canonical Allele Identifier: CA379888434

Gene: CSRP3

Linked Data

• MyVariant Identifiers: chr11:g.19209843T>A (hg19) ; chr11:g.19188296T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188296T>A , CM000673.2:g.19188296T>A	GRCh38
NC_000011.9:g.19209843T>A , CM000673.1:g.19209843T>A	GRCh37
NC_000011.8:g.19166419T>A	NCBI36
NG_011932.2:g.27278A>T , LRG_440:g.27278A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000265968.9:c.121A>T MANE Select	ENSP00000265968.3:p.Arg41Trp
ENST00000533783.2:c.121A>T	ENSP00000431813.1:p.Arg41Trp
ENST00000647990.1:c.121A>T	ENSP00000496798.1:p.Arg41Trp
ENST00000648719.1:c.113-3251A>T	ENSP00000497633.1:n.113-3251A>T
ENST00000649235.1:c.121A>T	ENSP00000497388.1:p.Arg41Trp
ENST00000649842.1:c.113-1948A>T	ENSP00000497531.1:n.113-1948A>T
ENST00000265968.7:c.121A>T	ENSP00000265968.3:p.Arg41Trp
ENST00000533783.1:c.121A>T	ENSP00000431813.1:p.Arg41Trp
NM_003476.4:c.121A>T	NP_003467.1:p.Arg41Trp
XM_024448698.1:c.113-1948A>T	XP_024304466.1:n.113-1948A>T
NM_001369404.1:c.113-1948A>T	NP_001356333.1:n.113-1948A>T
NM_003476.5:c.121A>T MANE Select	NP_003467.1:p.Arg41Trp