Canonical Allele Identifier: CA11947177

Gene: HTR4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.148543814A>G , CM000667.2:g.148543814A>G	GRCh38
NC_000005.9:g.147923377A>G , CM000667.1:g.147923377A>G	GRCh37
NC_000005.8:g.147903570A>G	NCBI36
NG_029052.1:g.115363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000521530.6:c.353+4854T>C	ENSP00000428320.1:n.353+4854T>C
ENST00000377888.8:c.353+4854T>C MANE Select	ENSP00000367120.4:n.353+4854T>C
ENST00000360693.7:c.353+4854T>C	ENSP00000353915.3:n.353+4854T>C
ENST00000362016.6:c.353+4854T>C	ENSP00000355037.3:n.353+4854T>C
ENST00000377888.7:c.353+4854T>C	ENSP00000367120.3:n.353+4854T>C
ENST00000517929.5:c.353+4854T>C	ENSP00000435904.1:n.353+4854T>C
ENST00000520514.5:c.353+4854T>C	ENSP00000427913.1:n.353+4854T>C
ENST00000521124.5:n.359+4854T>C
ENST00000521530.5:c.353+4854T>C	ENSP00000428320.1:n.353+4854T>C
ENST00000521735.5:c.353+4854T>C	ENSP00000430979.1:n.353+4854T>C
ENST00000522588.5:c.353+4854T>C	ENSP00000430874.1:n.353+4854T>C
ENST00000524063.3:c.353+4854T>C	ENSP00000430451.1:n.353+4854T>C
ENST00000631296.1:c.353+4854T>C	ENSP00000485747.1:n.353+4854T>C
NM_000870.6:c.353+4854T>C	NP_000861.1:n.353+4854T>C
NM_001040169.2:c.353+4854T>C	NP_001035259.1:n.353+4854T>C
NM_001040172.2:c.353+4854T>C	NP_001035262.2:n.353+4854T>C
NM_001040173.2:c.353+4854T>C	NP_001035263.1:n.353+4854T>C
NM_001286410.1:c.353+4854T>C	NP_001273339.1:n.353+4854T>C
NM_199453.3:c.353+4854T>C	NP_955525.1:n.353+4854T>C
NR_104445.1:n.866+4854T>C
XR_001742935.1:n.777-6271A>G
NM_000870.7:c.353+4854T>C MANE Select	NP_000861.1:n.353+4854T>C
NR_104445.2:n.866+4854T>C