Canonical Allele Identifier: CA8411597

Gene: LRRC75A SNHG29

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16443936C>T , CM000679.2:g.16443936C>T	GRCh38
NC_000017.10:g.16347250C>T , CM000679.1:g.16347250C>T	GRCh37
NC_000017.9:g.16287975C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470794.2:c.687G>A (LRRC75A) MANE Select	ENSP00000419502.1:p.Leu229=
ENST00000409083.7:c.571G>A (LRRC75A)	ENSP00000386504.3:p.Ala191Thr
ENST00000409887.3:n.798G>A (LRRC75A)
ENST00000470794.1:c.687G>A (LRRC75A)	ENSP00000419502.1:p.Leu229=
NM_001113567.2:c.687G>A (LRRC75A)	NP_001107039.1:p.Leu229=
NM_207387.3:c.571G>A (LRRC75A)	NP_997270.2:p.Ala191Thr
NR_027171.1:n.554+2806C>T (SNHG29)
NR_027172.2:n.257+2806C>T (SNHG29)
NR_027173.1:n.288+2806C>T (SNHG29)
NR_027174.1:n.288+2806C>T (SNHG29)
NR_027175.1:n.288+2806C>T (SNHG29)
NR_027176.1:n.231+3683C>T (SNHG29)
NR_027177.1:n.288+2806C>T (SNHG29)
NR_027178.1:n.288+2806C>T (SNHG29)
NR_045023.1:n.231+3683C>T (SNHG29)
NR_045025.1:n.200+2806C>T (SNHG29)
XM_011523845.1:c.*239G>A (LRRC75A)	XP_011522147.1:n.*239G>A
XM_011523845.3:c.*239G>A (LRRC75A)	XP_011522147.1:n.*239G>A
XM_017024619.1:c.642G>A (LRRC75A)	XP_016880108.1:p.Leu214=
XM_017024620.1:c.561G>A (LRRC75A)	XP_016880109.1:p.Leu187=
NM_001113567.3:c.687G>A (LRRC75A) MANE Select	NP_001107039.1:p.Leu229=
NM_207387.4:c.571G>A (LRRC75A)	NP_997270.2:p.Ala191Thr