Canonical Allele Identifier: CA497388884

Gene: PRPF8

Linked Data

• gnomAD v4: 17-1651169-C-G
• MyVariant Identifiers: chr17:g.1554463C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1651169C>G , CM000679.2:g.1651169C>G	GRCh38
NC_000017.10:g.1554463C>G , CM000679.1:g.1554463C>G	GRCh37
NC_000017.9:g.1501213C>G	NCBI36
NG_009118.1:g.38714G>C
NG_033061.1:g.3930G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000573725.2:c.6612G>C	ENSP00000460849.2:p.Ser2204=
ENST00000703537.1:c.2540G>C
ENST00000703538.1:c.*6515G>C	ENSP00000515361.1:n.*6515G>C
ENST00000703539.1:n.3106G>C
ENST00000703540.1:c.6645G>C	ENSP00000515362.1:p.Ser2215=
ENST00000703541.1:c.6657G>C	ENSP00000515363.1:p.Ser2219=
ENST00000304992.11:c.6792G>C MANE Select	ENSP00000304350.6:p.Ser2264=
ENST00000304992.10:c.6792G>C	ENSP00000304350.6:p.Ser2264=
ENST00000571958.1:c.101G>C
ENST00000572621.5:c.6792G>C	ENSP00000460348.1:p.Ser2264=
ENST00000572723.1:n.781G>C
NM_006445.3:c.6792G>C	NP_006436.3:p.Ser2264=
XM_024450537.1:c.6792G>C	XP_024306305.1:p.Ser2264=
NM_006445.4:c.6792G>C MANE Select	NP_006436.3:p.Ser2264=