Canonical Allele Identifier: CA379888451

Gene: CSRP3

Linked Data

• MyVariant Identifiers: chr11:g.19209852C>A (hg19) ; chr11:g.19188305C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19188305C>A , CM000673.2:g.19188305C>A	GRCh38
NC_000011.9:g.19209852C>A , CM000673.1:g.19209852C>A	GRCh37
NC_000011.8:g.19166428C>A	NCBI36
NG_011932.2:g.27269G>T , LRG_440:g.27269G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.113-1G>T MANE Select	ENSP00000265968.3:n.113-1G>T
ENST00000533783.2:c.113-1G>T	ENSP00000431813.1:n.113-1G>T
ENST00000647990.1:c.113-1G>T	ENSP00000496798.1:n.113-1G>T
ENST00000648719.1:c.113-3260G>T	ENSP00000497633.1:n.113-3260G>T
ENST00000649235.1:c.113-1G>T	ENSP00000497388.1:n.113-1G>T
ENST00000649842.1:c.113-1957G>T	ENSP00000497531.1:n.113-1957G>T
ENST00000265968.7:c.113-1G>T	ENSP00000265968.3:n.113-1G>T
ENST00000533783.1:c.113-1G>T	ENSP00000431813.1:n.113-1G>T
NM_003476.4:c.113-1G>T	NP_003467.1:n.113-1G>T
XM_024448698.1:c.113-1957G>T	XP_024304466.1:n.113-1957G>T
NM_001369404.1:c.113-1957G>T	NP_001356333.1:n.113-1957G>T
NM_003476.5:c.113-1G>T MANE Select	NP_003467.1:n.113-1G>T