Canonical Allele Identifier: CA401085841

Gene: SRP68

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.76067257T>C , CM000679.2:g.76067257T>C	GRCh38
NC_000017.10:g.74063338T>C , CM000679.1:g.74063338T>C	GRCh37
NC_000017.9:g.71574933T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307877.7:c.325A>G MANE Select	ENSP00000312066.1:p.Thr109Ala
ENST00000307877.6:c.325A>G	ENSP00000312066.1:p.Thr109Ala
ENST00000539137.5:c.252-3086A>G	ENSP00000446136.1:n.252-3086A>G
ENST00000591272.1:c.*125A>G	ENSP00000467765.1:n.*125A>G
ENST00000592704.5:c.*56A>G	ENSP00000466791.1:n.*56A>G
NM_001260502.1:c.252-3086A>G	NP_001247431.1:n.252-3086A>G
NM_014230.3:c.325A>G	NP_055045.2:p.Thr109Ala
NR_048541.1:n.256A>G
NM_014230.4:c.325A>G MANE Select	NP_055045.2:p.Thr109Ala
NM_001260502.2:c.252-3086A>G	NP_001247431.1:n.252-3086A>G
NR_048541.2:n.247A>G