Canonical Allele Identifier: CA347938920

Gene: IL18RAP

Linked Data

• MyVariant Identifiers: chr2:g.103057792C>T (hg19) ; chr2:g.102441332C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.102441332C>T , CM000664.2:g.102441332C>T	GRCh38
NC_000002.11:g.103057792C>T , CM000664.1:g.103057792C>T	GRCh37
NC_000002.10:g.102424224C>T	NCBI36
NG_011481.1:g.27539C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687160.1:c.751C>T MANE Select	ENSP00000510345.1:p.Pro251Ser
ENST00000264260.6:c.751C>T	ENSP00000264260.2:p.Pro251Ser
ENST00000409369.1:c.325C>T	ENSP00000387201.1:p.Pro109Ser
NM_003853.3:c.751C>T	NP_003844.1:p.Pro251Ser
XM_011512087.1:c.325C>T	XP_011510389.1:p.Pro109Ser
XM_011512088.1:c.325C>T	XP_011510390.1:p.Pro109Ser
XM_011512089.1:c.751C>T	XP_011510391.1:p.Pro251Ser
XR_923052.1:n.1088C>T
XM_011512087.2:c.325C>T	XP_011510389.1:p.Pro109Ser
XM_011512088.2:c.325C>T	XP_011510390.1:p.Pro109Ser
XM_024453197.1:c.751C>T	XP_024308965.1:p.Pro251Ser
XM_024453198.1:c.751C>T	XP_024308966.1:p.Pro251Ser
XM_024453199.1:c.751C>T	XP_024308967.1:p.Pro251Ser
XM_024453200.1:c.751C>T	XP_024308968.1:p.Pro251Ser
XM_024453201.1:c.751C>T	XP_024308969.1:p.Pro251Ser
XR_001739011.2:n.1086C>T
NM_001393486.1:c.751C>T	NP_001380415.1:p.Pro251Ser
NM_001393487.1:c.751C>T MANE Select	NP_001380416.1:p.Pro251Ser
NM_001393488.1:c.325C>T	NP_001380417.1:p.Pro109Ser
NM_001393489.1:c.325C>T	NP_001380418.1:p.Pro109Ser
NM_003853.4:c.751C>T	NP_003844.1:p.Pro251Ser