Canonical Allele Identifier: CA14175579

Gene: ADAMTSL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.83911404G>A , CM000677.2:g.83911404G>A	GRCh38
NC_000015.9:g.84580156G>A , CM000677.1:g.84580156G>A	GRCh37
NC_000015.8:g.82371160G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286744.10:c.1701-1688G>A MANE Select	ENSP00000286744.5:n.1701-1688G>A
ENST00000286744.9:c.1701-1688G>A	ENSP00000286744.5:n.1701-1688G>A
ENST00000561483.5:n.1916-1688G>A
ENST00000567476.1:c.1701-1688G>A	ENSP00000456313.1:n.1701-1688G>A
NM_001301110.1:c.1701-1688G>A	NP_001288039.1:n.1701-1688G>A
NM_207517.2:c.1701-1688G>A	NP_997400.2:n.1701-1688G>A
XM_011521821.1:c.1782-1688G>A	XP_011520123.1:n.1782-1688G>A
XM_011521822.1:c.1782-1688G>A	XP_011520124.1:n.1782-1688G>A
XM_011521823.1:c.1782-1688G>A	XP_011520125.1:n.1782-1688G>A
XM_011521824.1:c.1782-1688G>A	XP_011520126.1:n.1782-1688G>A
XM_011521825.1:c.1782-1688G>A	XP_011520127.1:n.1782-1688G>A
XR_931873.1:n.1815-1688G>A
XM_011521822.2:c.1782-1688G>A	XP_011520124.1:n.1782-1688G>A
XM_011521823.2:c.1782-1688G>A	XP_011520125.1:n.1782-1688G>A
XM_011521824.2:c.1782-1688G>A	XP_011520126.1:n.1782-1688G>A
XM_011521825.2:c.1782-1688G>A	XP_011520127.1:n.1782-1688G>A
XM_017022434.1:c.1782-1688G>A	XP_016877923.1:n.1782-1688G>A
XM_017022435.1:c.1206-1688G>A	XP_016877924.1:n.1206-1688G>A
XM_024450000.1:c.1782-1688G>A	XP_024305768.1:n.1782-1688G>A
XR_931873.2:n.1997-1688G>A
NM_207517.3:c.1701-1688G>A MANE Select	NP_997400.2:n.1701-1688G>A
NM_001301110.2:c.1701-1688G>A	NP_001288039.1:n.1701-1688G>A