Canonical Allele Identifier: CA15176692

Gene: RNF149

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.101305708T>G , CM000664.2:g.101305708T>G	GRCh38
NC_000002.11:g.101922170T>G , CM000664.1:g.101922170T>G	GRCh37
NC_000002.10:g.101288602T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295317.4:c.460+2421A>C MANE Select	ENSP00000295317.3:n.460+2421A>C
ENST00000295317.3:c.460+2421A>C	ENSP00000295317.3:n.460+2421A>C
ENST00000424632.5:c.460+2421A>C	ENSP00000399090.1:n.460+2421A>C
NM_173647.3:c.460+2421A>C	NP_775918.2:n.460+2421A>C
XM_005263920.1:c.460+2421A>C	XP_005263977.1:n.460+2421A>C
XM_005263921.3:c.460+2421A>C	XP_005263978.1:n.460+2421A>C
XM_011510990.1:c.-24+2133A>C	XP_011509292.1:n.-24+2133A>C
XR_244888.2:n.588+2421A>C
XR_922908.1:n.588+2421A>C
XR_922909.1:n.588+2421A>C
XM_005263920.3:c.460+2421A>C	XP_005263977.1:n.460+2421A>C
XM_005263921.4:c.460+2421A>C	XP_005263978.1:n.460+2421A>C
XM_011510990.2:c.-24+2133A>C	XP_011509292.1:n.-24+2133A>C
XM_024452811.1:c.460+2421A>C	XP_024308579.1:n.460+2421A>C
XR_001738712.2:n.562+2421A>C
XR_001738713.2:n.562+2421A>C
XR_001738714.2:n.571+2421A>C
XR_244888.4:n.571+2421A>C
XR_922908.2:n.562+2421A>C
XR_922909.3:n.562+2421A>C
NM_173647.4:c.460+2421A>C MANE Select	NP_775918.2:n.460+2421A>C