Canonical Allele Identifier: CA11890542

Gene: LNX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.53464700A>G , CM000666.2:g.53464700A>G	GRCh38
NC_000004.11:g.54330867A>G , CM000666.1:g.54330867A>G	GRCh37
NC_000004.10:g.54025624A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263925.8:c.1893-3107T>C MANE Select	ENSP00000263925.7:n.1893-3107T>C
ENST00000263925.7:c.1893-3107T>C	ENSP00000263925.7:n.1893-3107T>C
ENST00000306888.6:c.1605-3107T>C	ENSP00000302879.2:n.1605-3107T>C
ENST00000507166.5:c.1017+38735A>G	ENSP00000423325.1:n.1017+38735A>G
NM_001126328.2:c.1893-3107T>C	NP_001119800.1:n.1893-3107T>C
NM_032622.2:c.1605-3107T>C	NP_116011.2:n.1605-3107T>C
XM_005265785.3:c.1893-3107T>C	XP_005265842.1:n.1893-3107T>C
XM_005265786.3:c.1893-3107T>C	XP_005265843.1:n.1893-3107T>C
XM_005265785.5:c.1893-3107T>C	XP_005265842.1:n.1893-3107T>C
XM_017008776.1:c.1893-3107T>C	XP_016864265.1:n.1893-3107T>C
XM_024454261.1:c.1893-3107T>C	XP_024310029.1:n.1893-3107T>C
XM_024454262.1:c.1893-3107T>C	XP_024310030.1:n.1893-3107T>C
NM_001126328.3:c.1893-3107T>C MANE Select	NP_001119800.1:n.1893-3107T>C
NM_032622.3:c.1605-3107T>C	NP_116011.2:n.1605-3107T>C