Canonical Allele Identifier: CA645600373
Gene: HRH4 HGNC NCBI

Linked Data

COSMIC: COSM5702432
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477217_24477218delinsTT , CM000680.2:g.24477217_24477218delinsTT GRCh38
NC_000018.9:g.22057181_22057182delinsTT , CM000680.1:g.22057181_22057182delinsTT GRCh37
NC_000018.8:g.20311179_20311180delinsTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.828_829delinsTT MANE Select ENSP00000256906.4:p.Met276_Gly277delinsIleCys
ENST00000256906.4:c.828_829delinsTT ENSP00000256906.4:p.Met276_Gly277delinsIleCys
ENST00000426880.2:c.564_565delinsTT ENSP00000402526.2:p.Met188_Gly189delinsIleCys
NM_001143828.1:c.564_565delinsTT NP_001137300.1:p.Met188_Gly189delinsIleCys
NM_001160166.1:c.*460_*461delinsTT NP_001153638.1:n.*460_*461delinsTT
NM_021624.3:c.828_829delinsTT NP_067637.2:p.Met276_Gly277delinsIleCys
XM_011526133.1:c.357+8266_357+8267delinsTT XP_011524435.1:n.357+8266_357+8267delinsTT
NM_021624.4:c.828_829delinsTT MANE Select NP_067637.2:p.Met276_Gly277delinsIleCys
NM_001143828.2:c.564_565delinsTT NP_001137300.1:p.Met188_Gly189delinsIleCys
NM_001160166.2:c.*460_*461delinsTT NP_001153638.1:n.*460_*461delinsTT
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