Canonical Allele Identifier: CA218632592

Gene: CSRP3

Linked Data

• dbSNP Id: rs969365639
• gnomAD v3: 11-19184845-A-T
• gnomAD v4: 11-19184845-A-T
• MyVariant Identifiers: chr11:g.19206392A>T (hg19) ; chr11:g.19184845A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19184845A>T , CM000673.2:g.19184845A>T	GRCh38
NC_000011.9:g.19206392A>T , CM000673.1:g.19206392A>T	GRCh37
NC_000011.8:g.19162968A>T	NCBI36
NG_011932.2:g.30729T>A , LRG_440:g.30729T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265968.9:c.508+107T>A MANE Select	ENSP00000265968.3:n.508+107T>A
ENST00000533783.2:c.508+107T>A	ENSP00000431813.1:n.508+107T>A
ENST00000647990.1:c.375+107T>A	ENSP00000496798.1:n.375+107T>A
ENST00000648719.1:c.*26+107T>A	ENSP00000497633.1:n.*26+107T>A
ENST00000649235.1:c.508+107T>A	ENSP00000497388.1:n.508+107T>A
ENST00000649842.1:c.339+107T>A	ENSP00000497531.1:n.339+107T>A
ENST00000265968.7:c.508+107T>A	ENSP00000265968.3:n.508+107T>A
ENST00000533783.1:c.508+107T>A	ENSP00000431813.1:n.508+107T>A
NM_003476.4:c.508+107T>A	NP_003467.1:n.508+107T>A
XM_024448698.1:c.339+107T>A	XP_024304466.1:n.339+107T>A
NM_001369404.1:c.339+107T>A	NP_001356333.1:n.339+107T>A
NM_003476.5:c.508+107T>A MANE Select	NP_003467.1:n.508+107T>A