Canonical Allele Identifier: CA7474888
Gene: SRP14 HGNC NCBI

Linked Data

ClinVar Variation Id: 402822
ClinVar RCV Id: RCV000454791
dbSNP Id: rs7535
ExAC: 15:40328575 G / C
gnomAD v2: 15-40328575-G-C
gnomAD v3: 15-40036374-G-C
gnomAD v4: 15-40036374-G-C
MyVariant Identifiers: chr15:g.40328575G>C (hg19) chr15:g.40036374G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40036374G>C , CM000677.2:g.40036374G>C GRCh38
NC_000015.9:g.40328575G>C , CM000677.1:g.40328575G>C GRCh37
NC_000015.8:g.38115867G>C NCBI36
NG_034053.1:g.107251G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000267884.11:c.370C>G MANE Select ENSP00000267884.6:p.Pro124Ala
ENST00000267884.10:c.370C>G ENSP00000267884.6:p.Pro124Ala
ENST00000558527.5:n.458C>G
ENST00000558720.5:c.130C>G ENSP00000453361.1:p.Pro44Ala
ENST00000559439.5:n.623C>G
ENST00000559475.5:n.393C>G
ENST00000560773.5:c.130C>G ENSP00000452756.1:p.Pro44Ala
NM_001309434.1:c.226C>G NP_001296363.1:p.Pro76Ala
NM_003134.4:c.370C>G NP_003125.3:p.Pro124Ala
NM_003134.5:c.370C>G NP_003125.3:p.Pro124Ala
NM_003134.6:c.370C>G MANE Select NP_003125.3:p.Pro124Ala
Search 100 bp 5'
Search 100 bp 3'