Canonical Allele Identifier: CA2746071785

Gene: PRPF3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150346613_150346614insAG , CM000663.2:g.150346613_150346614insAG	GRCh38
NC_000001.10:g.150319089_150319090insAG , CM000663.1:g.150319089_150319090insAG	GRCh37
NC_000001.9:g.148585713_148585714insAG	NCBI36
NG_008245.1:g.30162_30163insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324862.7:c.1843+122_1843+123insAG MANE Select	ENSP00000315379.6:n.1843+122_1843+123insAG
ENST00000324862.6:c.1843+122_1843+123insAG	ENSP00000315379.6:n.1843+122_1843+123insAG
ENST00000467329.5:n.2170+122_2170+123insAG
ENST00000476970.1:n.952+122_952+123insAG
NM_004698.2:c.1843+122_1843+123insAG	NP_004689.1:n.1843+122_1843+123insAG
XM_011510128.1:c.1853+112_1853+113insAG	XP_011508430.1:n.1853+112_1853+113insAG
XM_011510129.1:c.1438+122_1438+123insAG	XP_011508431.1:n.1438+122_1438+123insAG
XM_011510130.1:c.1411+122_1411+123insAG	XP_011508432.1:n.1411+122_1411+123insAG
XR_241103.1:n.1826+122_1826+123insAG
XR_921997.1:n.1836+112_1836+113insAG
XR_921998.1:n.1940+122_1940+123insAG
NM_001350529.1:c.1438+122_1438+123insAG	NP_001337458.1:n.1438+122_1438+123insAG
NM_004698.3:c.1843+122_1843+123insAG	NP_004689.1:n.1843+122_1843+123insAG
NR_146766.1:n.2074+122_2074+123insAG
NR_146767.1:n.2170+122_2170+123insAG
NR_146768.1:n.2026+112_2026+113insAG
NR_146769.1:n.2079+112_2079+113insAG
XM_011510130.3:c.1411+122_1411+123insAG	XP_011508432.1:n.1411+122_1411+123insAG
XM_017002790.1:c.1411+122_1411+123insAG	XP_016858279.1:n.1411+122_1411+123insAG
XR_001737536.2:n.1876+122_1876+123insAG
XR_001737537.2:n.1990+122_1990+123insAG
XR_001737540.2:n.2747+122_2747+123insAG
XR_001737541.2:n.1770+122_1770+123insAG
XR_002958009.1:n.2500+122_2500+123insAG
XR_002958010.1:n.3746+112_3746+113insAG
XR_002958012.1:n.1942+112_1942+113insAG
XR_241103.3:n.1818+122_1818+123insAG
XR_921997.3:n.1828+112_1828+113insAG
XR_921998.3:n.1932+122_1932+123insAG
NM_004698.4:c.1843+122_1843+123insAG MANE Select	NP_004689.1:n.1843+122_1843+123insAG