Canonical Allele Identifier: CA2405257914
Gene: SYNGR1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.39351666T>C , CM000684.2:g.39351666T>C GRCh38
NC_000022.10:g.39747671T>C , CM000684.1:g.39747671T>C GRCh37
NC_000022.9:g.38077617T>C NCBI36
NG_047102.1:g.6718T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000328933.10:c.99+1557T>C MANE Select ENSP00000332287.5:n.99+1557T>C
ENST00000216155.11:c.99+1557T>C ENSP00000216155.7:n.99+1557T>C
ENST00000318801.8:c.99+1557T>C ENSP00000318845.4:n.99+1557T>C
ENST00000328933.9:c.99+1557T>C ENSP00000332287.5:n.99+1557T>C
ENST00000406293.7:c.99+1557T>C ENSP00000385447.3:n.99+1557T>C
ENST00000415332.1:c.99+1557T>C ENSP00000412442.1:n.99+1557T>C
ENST00000489206.1:n.104+1557T>C
NM_004711.4:c.99+1557T>C NP_004702.2:n.99+1557T>C
NM_145731.3:c.99+1557T>C NP_663783.1:n.99+1557T>C
NM_004711.5:c.99+1557T>C MANE Select NP_004702.2:n.99+1557T>C
NM_145731.4:c.99+1557T>C NP_663783.1:n.99+1557T>C
Search 100 bp 5'
Search 100 bp 3'