Canonical Allele Identifier: CA367646962

Gene: SBDS

Linked Data

• MyVariant Identifiers: chr7:g.66456254A>C (hg19) ; chr7:g.66991267A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.66991267A>C , CM000669.2:g.66991267A>C	GRCh38
NC_000007.13:g.66456254A>C , CM000669.1:g.66456254A>C	GRCh37
NC_000007.12:g.66093689A>C	NCBI36
NG_007277.1:g.9335T>G , LRG_104:g.9335T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000414306.6:c.*225T>G	ENSP00000394586.1:n.*225T>G
ENST00000697860.1:n.461T>G
ENST00000697861.1:c.293T>G	ENSP00000513460.1:p.Met98Arg
ENST00000697862.1:c.460-45T>G	ENSP00000513461.1:n.460-45T>G
ENST00000697863.1:c.437T>G	ENSP00000513462.1:p.Met146Arg
ENST00000697864.1:n.1638T>G
ENST00000697865.1:c.437T>G	ENSP00000513463.1:p.Met146Arg
ENST00000697866.1:c.176T>G	ENSP00000513464.1:p.Met59Arg
ENST00000697867.1:c.334T>G
ENST00000697868.1:c.*258T>G	ENSP00000513466.1:n.*258T>G
ENST00000697897.1:c.494T>G	ENSP00000513469.1:p.Met165Arg
ENST00000246868.7:c.494T>G MANE Select	ENSP00000246868.2:p.Met165Arg
ENST00000246868.6:c.494T>G	ENSP00000246868.2:p.Met165Arg
ENST00000414306.5:c.*225T>G	ENSP00000394586.1:n.*225T>G
ENST00000463579.1:n.383T>G
ENST00000490953.5:n.635T>G
ENST00000617799.1:c.494T>G	ENSP00000483040.1:p.Met165Arg
NM_016038.2:c.494T>G , LRG_104t1:c.494T>G	NP_057122.2:p.Met165Arg
NM_016038.3:c.494T>G	NP_057122.2:p.Met165Arg
NM_016038.4:c.494T>G MANE Select	NP_057122.2:p.Met165Arg