Canonical Allele Identifier: CA726008087

Gene: SHISA6

Linked Data

• dbSNP Id: rs1228730828
• MyVariant Identifiers: chr17:g.11250301T>C (hg19) ; chr17:g.11346984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.11346984T>C , CM000679.2:g.11346984T>C	GRCh38
NC_000017.10:g.11250301T>C , CM000679.1:g.11250301T>C	GRCh37
NC_000017.9:g.11191026T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441885.8:c.800-32430T>C MANE Select	ENSP00000390084.3:n.800-32430T>C
ENST00000343478.7:c.282-32430T>C
ENST00000409168.7:c.799+83458T>C	ENSP00000387157.3:n.799+83458T>C
ENST00000432116.7:c.800-32430T>C	ENSP00000388659.3:n.800-32430T>C
ENST00000441885.7:c.800-32430T>C	ENSP00000390084.3:n.800-32430T>C
NM_001173461.1:c.799+83458T>C	NP_001166932.1:n.799+83458T>C
NM_001173462.1:c.800-32430T>C	NP_001166933.1:n.800-32430T>C
NM_207386.3:c.800-32430T>C	NP_997269.2:n.800-32430T>C
XM_011523837.1:c.800-32430T>C	XP_011522139.1:n.800-32430T>C
XM_017024618.1:c.799+83458T>C	XP_016880107.1:n.799+83458T>C
NM_001173462.2:c.800-32430T>C	NP_001166933.1:n.800-32430T>C
NM_207386.4:c.800-32430T>C MANE Select	NP_997269.2:n.800-32430T>C