Canonical Allele Identifier: CA13479112

Gene: CSRP3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19192211A>G , CM000673.2:g.19192211A>G	GRCh38
NC_000011.9:g.19213758A>G , CM000673.1:g.19213758A>G	GRCh37
NC_000011.8:g.19170334A>G	NCBI36
NG_011932.2:g.23363T>C , LRG_440:g.23363T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003476.5:c.112+126T>C MANE Select	NP_003467.1:n.112+126T>C
ENST00000265968.9:c.112+126T>C MANE Select	ENSP00000265968.3:n.112+126T>C
NM_001369404.1:c.112+126T>C	NP_001356333.1:n.112+126T>C
NM_003476.4:c.112+126T>C	NP_003467.1:n.112+126T>C
ENST00000265968.7:c.112+126T>C	ENSP00000265968.3:n.112+126T>C
ENST00000533783.1:c.112+126T>C	ENSP00000431813.1:n.112+126T>C
ENST00000533783.2:c.112+126T>C	ENSP00000431813.1:n.112+126T>C
ENST00000647990.1:c.112+126T>C	ENSP00000496798.1:n.112+126T>C
ENST00000648719.1:c.112+126T>C	ENSP00000497633.1:n.112+126T>C
ENST00000649235.1:c.112+126T>C	ENSP00000497388.1:n.112+126T>C
ENST00000649842.1:c.112+126T>C	ENSP00000497531.1:n.112+126T>C
XM_024448698.1:c.112+126T>C	XP_024304466.1:n.112+126T>C