Canonical Allele Identifier: CA11704400

Gene: FHDC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.152972202G>A , CM000666.2:g.152972202G>A	GRCh38
NC_000004.11:g.153893354G>A , CM000666.1:g.153893354G>A	GRCh37
NC_000004.10:g.154112804G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511601.6:c.1219-175G>A MANE Select	ENSP00000427567.1:n.1219-175G>A
ENST00000260008.3:c.1219-175G>A	ENSP00000260008.3:n.1219-175G>A
ENST00000511601.5:c.1219-175G>A	ENSP00000427567.1:n.1219-175G>A
NM_033393.2:c.1219-175G>A	NP_203751.2:n.1219-175G>A
XM_005263319.2:c.1219-175G>A	XP_005263376.1:n.1219-175G>A
XM_006714393.2:c.1219-175G>A	XP_006714456.1:n.1219-175G>A
XM_006714394.2:c.217-175G>A	XP_006714457.1:n.217-175G>A
XM_011532388.1:c.1219-175G>A	XP_011530690.1:n.1219-175G>A
XM_011532389.1:c.1219-175G>A	XP_011530691.1:n.1219-175G>A
XM_005263319.3:c.1219-175G>A	XP_005263376.1:n.1219-175G>A
XM_006714393.3:c.1219-175G>A	XP_006714456.1:n.1219-175G>A
NM_001371116.1:c.1219-175G>A MANE Select	NP_001358045.1:n.1219-175G>A
NM_033393.3:c.1219-175G>A	NP_203751.2:n.1219-175G>A