Canonical Allele Identifier: CA16577655

Gene: SHLD1

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.5859893A>G , CM000682.2:g.5859893A>G	GRCh38
NC_000020.10:g.5840539A>G , CM000682.1:g.5840539A>G	GRCh37
NC_000020.9:g.5788539A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000303142.11:c.179-3131A>G MANE Select	ENSP00000305875.6:n.179-3131A>G
ENST00000303142.10:c.179-3131A>G	ENSP00000305875.6:n.179-3131A>G
ENST00000442185.1:c.320-3131A>G	ENSP00000410534.1:n.320-3131A>G
ENST00000445603.1:c.179-3131A>G	ENSP00000399331.1:n.179-3131A>G
NM_001303477.1:c.179-3131A>G	NP_001290406.1:n.179-3131A>G
NM_001303478.1:c.83-3131A>G	NP_001290407.1:n.83-3131A>G
NM_152504.3:c.179-3131A>G	NP_689717.2:n.179-3131A>G
XM_006723549.2:c.185-3131A>G	XP_006723612.1:n.185-3131A>G
XM_011529177.1:c.218-3131A>G	XP_011527479.1:n.218-3131A>G
XM_006723549.4:c.185-3131A>G	XP_006723612.1:n.185-3131A>G
XM_011529177.2:c.218-3131A>G	XP_011527479.1:n.218-3131A>G
XM_017027684.1:c.179-3131A>G	XP_016883173.1:n.179-3131A>G
NM_152504.4:c.179-3131A>G MANE Select	NP_689717.2:n.179-3131A>G
NM_001303477.2:c.179-3131A>G	NP_001290406.1:n.179-3131A>G
NM_001303478.2:c.83-3131A>G	NP_001290407.1:n.83-3131A>G