Canonical Allele Identifier: CA645600374
Gene: HRH4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.24477304_24477305delinsTT , CM000680.2:g.24477304_24477305delinsTT GRCh38
NC_000018.9:g.22057268_22057269delinsTT , CM000680.1:g.22057268_22057269delinsTT GRCh37
NC_000018.8:g.20311266_20311267delinsTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256906.5:c.915_916delinsTT MANE Select ENSP00000256906.4:p.Ala306Ser
ENST00000256906.4:c.915_916delinsTT ENSP00000256906.4:p.Ala306Ser
ENST00000426880.2:c.651_652delinsTT ENSP00000402526.2:p.Ala218Ser
NM_001143828.1:c.651_652delinsTT NP_001137300.1:p.Ala218Ser
NM_001160166.1:c.*547_*548delinsTT NP_001153638.1:n.*547_*548delinsTT
NM_021624.3:c.915_916delinsTT NP_067637.2:p.Ala306Ser
XM_011526133.1:c.357+8353_357+8354delinsTT XP_011524435.1:n.357+8353_357+8354delinsTT
NM_021624.4:c.915_916delinsTT MANE Select NP_067637.2:p.Ala306Ser
NM_001143828.2:c.651_652delinsTT NP_001137300.1:p.Ala218Ser
NM_001160166.2:c.*547_*548delinsTT NP_001153638.1:n.*547_*548delinsTT