Canonical Allele Identifier: CA14396021

Gene: SHISA6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.11439291G>A , CM000679.2:g.11439291G>A	GRCh38
NC_000017.10:g.11342608G>A , CM000679.1:g.11342608G>A	GRCh37
NC_000017.9:g.11283333G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000441885.8:c.895+59782G>A MANE Select	ENSP00000390084.3:n.895+59782G>A
ENST00000409168.7:c.800-116449G>A	ENSP00000387157.3:n.800-116449G>A
ENST00000432116.7:c.895+59782G>A	ENSP00000388659.3:n.895+59782G>A
ENST00000441885.7:c.895+59782G>A	ENSP00000390084.3:n.895+59782G>A
NM_001173461.1:c.800-116449G>A	NP_001166932.1:n.800-116449G>A
NM_001173462.1:c.895+59782G>A	NP_001166933.1:n.895+59782G>A
NM_207386.3:c.895+59782G>A	NP_997269.2:n.895+59782G>A
XM_011523837.1:c.895+59782G>A	XP_011522139.1:n.895+59782G>A
XM_017024618.1:c.800-112605G>A	XP_016880107.1:n.800-112605G>A
NM_001173462.2:c.895+59782G>A	NP_001166933.1:n.895+59782G>A
NM_207386.4:c.895+59782G>A MANE Select	NP_997269.2:n.895+59782G>A