Canonical Allele Identifier: CA2838255467

Gene: LRRC75A SNHG29

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16444151A>G , CM000679.2:g.16444151A>G	GRCh38
NC_000017.10:g.16347465A>G , CM000679.1:g.16347465A>G	GRCh37
NC_000017.9:g.16288190A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470794.2:c.492-20T>C (LRRC75A) MANE Select	ENSP00000419502.1:n.492-20T>C
ENST00000409083.7:c.376-20T>C (LRRC75A)	ENSP00000386504.3:n.376-20T>C
ENST00000409887.3:n.603-20T>C (LRRC75A)
ENST00000470794.1:c.492-20T>C (LRRC75A)	ENSP00000419502.1:n.492-20T>C
NM_001113567.2:c.492-20T>C (LRRC75A)	NP_001107039.1:n.492-20T>C
NM_207387.3:c.376-20T>C (LRRC75A)	NP_997270.2:n.376-20T>C
NR_027171.1:n.554+3021A>G (SNHG29)
NR_027172.2:n.257+3021A>G (SNHG29)
NR_027173.1:n.288+3021A>G (SNHG29)
NR_027174.1:n.288+3021A>G (SNHG29)
NR_027175.1:n.288+3021A>G (SNHG29)
NR_027176.1:n.231+3898A>G (SNHG29)
NR_027177.1:n.288+3021A>G (SNHG29)
NR_027178.1:n.288+3021A>G (SNHG29)
NR_045023.1:n.231+3898A>G (SNHG29)
NR_045025.1:n.200+3021A>G (SNHG29)
XM_011523845.1:c.*44-20T>C (LRRC75A)	XP_011522147.1:n.*44-20T>C
XM_011523845.3:c.*44-20T>C (LRRC75A)	XP_011522147.1:n.*44-20T>C
XM_017024619.1:c.447-20T>C (LRRC75A)	XP_016880108.1:n.447-20T>C
XM_017024620.1:c.366-20T>C (LRRC75A)	XP_016880109.1:n.366-20T>C
NM_001113567.3:c.492-20T>C (LRRC75A) MANE Select	NP_001107039.1:n.492-20T>C
NM_207387.4:c.376-20T>C (LRRC75A)	NP_997270.2:n.376-20T>C