Canonical Allele Identifier: CA1590060732
Gene: HTR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.148476770G= , CM000667.2:g.148476770G= GRCh38
NC_000005.9:g.147856333G= , CM000667.1:g.147856333G= GRCh37
NC_000005.8:g.147836526G= NCBI36
NG_029052.1:g.182407C=

Transcript Alleles

HGVS Amino-acid Change
NM_001040169.2:c.1077-25498C= NP_001035259.1:n.1077-25498C=
NM_001040172.2:c.1077-25C= NP_001035262.2:n.1077-25C=
NM_199453.3:c.1077-10845C= NP_955525.1:n.1077-10845C=
ENST00000517929.5:c.1077-25C= ENSP00000435904.1:n.1077-25C=
ENST00000521530.5:c.1077-25498C= ENSP00000428320.1:n.1077-25498C=
ENST00000521530.6:c.1077-25498C= ENSP00000428320.1:n.1077-25498C=
ENST00000521735.5:c.1077-10845C= ENSP00000430979.1:n.1077-10845C=
ENST00000522588.5:c.1077-10845C= ENSP00000430874.1:n.1077-10845C=
XR_001742935.1:n.776+7753G=