Canonical Allele Identifier: CA2546360764

Gene: LRPPRC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.43918248_43918249insAAAGG , CM000664.2:g.43918248_43918249insAAAGG	GRCh38
NC_000002.11:g.44145387_44145388insAAAGG , CM000664.1:g.44145387_44145388insAAAGG	GRCh37
NC_000002.10:g.43998891_43998892insAAAGG	NCBI36
NG_008247.1:g.82757_82758insCCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000681993.1:n.591+7_591+8insCCTTT
ENST00000682295.1:c.303+7_303+8insCCTTT	ENSP00000507499.1:n.303+7_303+8insCCTTT
ENST00000682303.1:c.*2825+7_*2825+8insCCTTT	ENSP00000508325.1:n.*2825+7_*2825+8insCCT...
ENST00000682308.1:c.3039+7_3039+8insCCTTT	ENSP00000507056.1:n.3039+7_3039+8insCCTTT...
ENST00000682480.1:c.3039+7_3039+8insCCTTT	ENSP00000508344.1:n.3039+7_3039+8insCCTTT...
ENST00000682546.1:c.3036+7_3036+8insCCTTT	ENSP00000508188.1:n.3036+7_3036+8insCCTTT...
ENST00000682585.1:c.3039+7_3039+8insCCTTT	ENSP00000506885.1:n.3039+7_3039+8insCCTTT...
ENST00000682595.1:n.3623+7_3623+8insCCTTT
ENST00000682607.1:c.1457+7_1457+8insCCTTT
ENST00000682779.1:c.3030+7_3030+8insCCTTT	ENSP00000507947.1:n.3030+7_3030+8insCCTTT...
ENST00000682845.1:n.2141+7_2141+8insCCTTT
ENST00000682885.1:c.2994+7_2994+8insCCTTT	ENSP00000508036.1:n.2994+7_2994+8insCCTTT...
ENST00000682933.1:n.3113+7_3113+8insCCTTT
ENST00000683072.1:n.3623+7_3623+8insCCTTT
ENST00000683080.1:n.658+7_658+8insCCTTT
ENST00000683125.1:c.3147+7_3147+8insCCTTT	ENSP00000507939.1:n.3147+7_3147+8insCCTTT...
ENST00000683213.1:c.3042+7_3042+8insCCTTT	ENSP00000507751.1:n.3042+7_3042+8insCCTTT...
ENST00000683220.1:c.3069+7_3069+8insCCTTT	ENSP00000507151.1:n.3069+7_3069+8insCCTTT...
ENST00000683329.1:n.3842+7_3842+8insCCTTT
ENST00000683346.1:c.*2914+7_*2914+8insCCTTT	ENSP00000507458.1:n.*2914+7_*2914+8insCCT...
ENST00000683409.1:n.1646+7_1646+8insCCTTT
ENST00000683459.1:n.3626+7_3626+8insCCTTT
ENST00000683590.1:c.2897-5691_2897-5690insCCTTT	ENSP00000506820.1:n.2897-5691_2897-5690in...
ENST00000683623.1:c.2946+7_2946+8insCCTTT	ENSP00000507702.1:n.2946+7_2946+8insCCTTT...
ENST00000683645.1:n.3590+7_3590+8insCCTTT
ENST00000683796.1:c.*2911+7_*2911+8insCCTTT	ENSP00000508221.1:n.*2911+7_*2911+8insCCT...
ENST00000683802.1:n.5964+7_5964+8insCCTTT
ENST00000683833.1:c.3030+7_3030+8insCCTTT	ENSP00000506852.1:n.3030+7_3030+8insCCTTT...
ENST00000683994.1:c.3039+7_3039+8insCCTTT	ENSP00000507181.1:n.3039+7_3039+8insCCTTT...
ENST00000684290.1:c.*575+7_*575+8insCCTTT	ENSP00000507243.1:n.*575+7_*575+8insCCTTT...
ENST00000684306.1:c.*2952+7_*2952+8insCCTTT	ENSP00000508384.1:n.*2952+7_*2952+8insCCT...
ENST00000684341.1:n.3059+7_3059+8insCCTTT
ENST00000684383.1:c.*2677+7_*2677+8insCCTTT	ENSP00000506863.1:n.*2677+7_*2677+8insCCT...
ENST00000684619.1:c.*2911+7_*2911+8insCCTTT	ENSP00000508088.1:n.*2911+7_*2911+8insCCT...
ENST00000684705.1:n.160+7_160+8insCCTTT
ENST00000684743.1:n.4070+7_4070+8insCCTTT
ENST00000260665.12:c.3039+7_3039+8insCCTTT MANE Select	ENSP00000260665.7:n.3039+7_3039+8insCCTTT...
ENST00000260665.11:c.3039+7_3039+8insCCTTT	ENSP00000260665.7:n.3039+7_3039+8insCCTTT...
NM_133259.3:c.3039+7_3039+8insCCTTT	NP_573566.2:n.3039+7_3039+8insCCTTT
XM_006711915.2:c.2961+7_2961+8insCCTTT	XP_006711978.1:n.2961+7_2961+8insCCTTT
XM_006711916.2:c.3039+7_3039+8insCCTTT	XP_006711979.1:n.3039+7_3039+8insCCTTT
XM_011532473.1:c.3039+7_3039+8insCCTTT	XP_011530775.1:n.3039+7_3039+8insCCTTT
XM_011532474.1:c.3039+7_3039+8insCCTTT	XP_011530776.1:n.3039+7_3039+8insCCTTT
XM_006711916.3:c.3039+7_3039+8insCCTTT	XP_006711979.1:n.3039+7_3039+8insCCTTT
XM_017003117.1:c.2961+7_2961+8insCCTTT	XP_016858606.1:n.2961+7_2961+8insCCTTT
XR_002958896.1:n.3081+7_3081+8insCCTTT
NM_133259.4:c.3039+7_3039+8insCCTTT MANE Select	NP_573566.2:n.3039+7_3039+8insCCTTT