Canonical Allele Identifier: CA248837

Gene: RASAL3

Linked Data

• ClinVar Variation Id: 218343
• ClinVar RCV Id: RCV000202570
• dbSNP Id: rs76267899
• MyVariant Identifiers: chr19:g.15575174G>C (hg19) ; chr19:g.15464363G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.15464363G>C , CM000681.2:g.15464363G>C	GRCh38
NC_000019.9:g.15575174G>C , CM000681.1:g.15575174G>C	GRCh37
NC_000019.8:g.15436174G>C	NCBI36
NG_052951.1:g.5219C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343625.12:c.-5C>G MANE Select	ENSP00000341905.5:n.-5C>G
ENST00000343625.11:c.-5C>G	ENSP00000341905.5:n.-5C>G
ENST00000602101.6:n.25C>G
NM_022904.1:c.-5C>G	NP_075055.1:n.-5C>G
XM_011528185.1:c.-5C>G	XP_011526487.1:n.-5C>G
XM_011528186.1:c.-5C>G	XP_011526488.1:n.-5C>G
XM_011528187.1:c.-5C>G	XP_011526489.1:n.-5C>G
XR_936202.1:n.82C>G
XR_936203.1:n.82C>G
NM_001348027.1:c.-5C>G	NP_001334956.1:n.-5C>G
NM_001348028.1:c.-5C>G	NP_001334957.1:n.-5C>G
NM_022904.2:c.-5C>G	NP_075055.1:n.-5C>G
XM_024451656.1:c.-5C>G	XP_024307424.1:n.-5C>G
XR_001753737.1:n.82C>G
XR_936203.2:n.82C>G
NM_022904.3:c.-5C>G MANE Select	NP_075055.1:n.-5C>G
NM_001348027.2:c.-5C>G	NP_001334956.1:n.-5C>G
NM_001348028.2:c.-5C>G	NP_001334957.1:n.-5C>G
NM_001400377.1:c.-5C>G	NP_001387306.1:n.-5C>G
NM_001400378.1:c.-5C>G	NP_001387307.1:n.-5C>G
NM_001400379.1:c.-5C>G	NP_001387308.1:n.-5C>G
NM_001400380.1:c.-5C>G	NP_001387309.1:n.-5C>G
NM_001400381.1:c.-5C>G	NP_001387310.1:n.-5C>G
NR_174477.1:n.55C>G
NR_174478.1:n.55C>G