Canonical Allele Identifier: CA14927681

Gene: SYNGR1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000328933.10:c.99+1557T>A MANE Select	ENSP00000332287.5:n.99+1557T>A
ENST00000216155.11:c.99+1557T>A	ENSP00000216155.7:n.99+1557T>A
ENST00000318801.8:c.99+1557T>A	ENSP00000318845.4:n.99+1557T>A
ENST00000328933.9:c.99+1557T>A	ENSP00000332287.5:n.99+1557T>A
ENST00000406293.7:c.99+1557T>A	ENSP00000385447.3:n.99+1557T>A
ENST00000415332.1:c.99+1557T>A	ENSP00000412442.1:n.99+1557T>A
ENST00000489206.1:n.104+1557T>A
NM_004711.4:c.99+1557T>A	NP_004702.2:n.99+1557T>A
NM_145731.3:c.99+1557T>A	NP_663783.1:n.99+1557T>A
NM_004711.5:c.99+1557T>A MANE Select	NP_004702.2:n.99+1557T>A
NM_145731.4:c.99+1557T>A	NP_663783.1:n.99+1557T>A