Canonical Allele Identifier: CA1873319450

Gene: PRPF4

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113288272A= , CM000671.2:g.113288272A=	GRCh38
NC_000009.11:g.116050552A= , CM000671.1:g.116050552A=	GRCh37
NC_000009.10:g.115090373A=	NCBI36
NG_034225.1:g.17639A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374198.5:c.1022+8A= MANE Select	ENSP00000363313.4:n.1022+8A=
ENST00000374199.9:c.1025+8A=	ENSP00000363315.4:n.1025+8A=
ENST00000374198.4:c.1025+8A=	ENSP00000363313.3:n.1025+8A=
ENST00000374199.8:c.1022+8A=	ENSP00000363315.3:n.1022+8A=
NM_001244926.1:c.1022+8A=	NP_001231855.1:n.1022+8A=
NM_004697.4:c.1025+8A=	NP_004688.2:n.1025+8A=
XM_005252300.2:c.296+8A=	XP_005252357.1:n.296+8A=
XM_011519181.1:c.1025+8A=	XP_011517483.1:n.1025+8A=
NM_001322266.1:c.296+8A=	NP_001309195.1:n.296+8A=
NM_001322267.1:c.296+8A=	NP_001309196.1:n.296+8A=
NR_136265.1:n.1135+8A=
NR_136266.1:n.1132+8A=
NM_001244926.2:c.1022+8A= MANE Select	NP_001231855.1:n.1022+8A=
NM_001322266.2:c.296+8A=	NP_001309195.1:n.296+8A=
NM_001322267.2:c.296+8A=	NP_001309196.1:n.296+8A=
NM_004697.5:c.1025+8A=	NP_004688.2:n.1025+8A=
NR_136265.2:n.1111+8A=
NR_136266.2:n.1108+8A=