Canonical Allele Identifier: CA427840520

Gene: IL18RAP

Linked Data

• MyVariant Identifiers: chr2:g.103057809T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102441349T>C , CM000664.2:g.102441349T>C	GRCh38
NC_000002.11:g.103057809T>C , CM000664.1:g.103057809T>C	GRCh37
NC_000002.10:g.102424241T>C	NCBI36
NG_011481.1:g.27556T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.768T>C MANE Select	ENSP00000510345.1:p.Pro256=
ENST00000264260.6:c.768T>C	ENSP00000264260.2:p.Pro256=
ENST00000409369.1:c.342T>C	ENSP00000387201.1:p.Pro114=
NM_003853.3:c.768T>C	NP_003844.1:p.Pro256=
XM_011512087.1:c.342T>C	XP_011510389.1:p.Pro114=
XM_011512088.1:c.342T>C	XP_011510390.1:p.Pro114=
XM_011512089.1:c.768T>C	XP_011510391.1:p.Pro256=
XR_923052.1:n.1105T>C
XM_011512087.2:c.342T>C	XP_011510389.1:p.Pro114=
XM_011512088.2:c.342T>C	XP_011510390.1:p.Pro114=
XM_024453197.1:c.768T>C	XP_024308965.1:p.Pro256=
XM_024453198.1:c.768T>C	XP_024308966.1:p.Pro256=
XM_024453199.1:c.768T>C	XP_024308967.1:p.Pro256=
XM_024453200.1:c.768T>C	XP_024308968.1:p.Pro256=
XM_024453201.1:c.768T>C	XP_024308969.1:p.Pro256=
XR_001739011.2:n.1103T>C
NM_001393486.1:c.768T>C	NP_001380415.1:p.Pro256=
NM_001393487.1:c.768T>C MANE Select	NP_001380416.1:p.Pro256=
NM_001393488.1:c.342T>C	NP_001380417.1:p.Pro114=
NM_001393489.1:c.342T>C	NP_001380418.1:p.Pro114=
NM_003853.4:c.768T>C	NP_003844.1:p.Pro256=