Canonical Allele Identifier: CA2612792271

Gene: CSRP3

Linked Data

• gnomAD v4: 11-19184847-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184847A>G , CM000673.2:g.19184847A>G	GRCh38
NC_000011.9:g.19206394A>G , CM000673.1:g.19206394A>G	GRCh37
NC_000011.8:g.19162970A>G	NCBI36
NG_011932.2:g.30727T>C , LRG_440:g.30727T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.508+105T>C MANE Select	ENSP00000265968.3:n.508+105T>C
ENST00000533783.2:c.508+105T>C	ENSP00000431813.1:n.508+105T>C
ENST00000647990.1:c.375+105T>C	ENSP00000496798.1:n.375+105T>C
ENST00000648719.1:c.*26+105T>C	ENSP00000497633.1:n.*26+105T>C
ENST00000649235.1:c.508+105T>C	ENSP00000497388.1:n.508+105T>C
ENST00000649842.1:c.339+105T>C	ENSP00000497531.1:n.339+105T>C
ENST00000265968.7:c.508+105T>C	ENSP00000265968.3:n.508+105T>C
ENST00000533783.1:c.508+105T>C	ENSP00000431813.1:n.508+105T>C
NM_003476.4:c.508+105T>C	NP_003467.1:n.508+105T>C
XM_024448698.1:c.339+105T>C	XP_024304466.1:n.339+105T>C
NM_001369404.1:c.339+105T>C	NP_001356333.1:n.339+105T>C
NM_003476.5:c.508+105T>C MANE Select	NP_003467.1:n.508+105T>C