Canonical Allele Identifier: CA339887

Gene: HYCC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.22977340C>A , CM000669.2:g.22977340C>A	GRCh38
NC_000007.13:g.23016959C>A , CM000669.1:g.23016959C>A	GRCh37
NC_000007.12:g.22983484C>A	NCBI36
NG_008392.1:g.41812G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432176.7:c.414+1G>T MANE Select	ENSP00000403396.2:n.414+1G>T
ENST00000440481.6:c.-19+1G>T	ENSP00000397168.2:n.-19+1G>T
ENST00000465661.2:n.605+1G>T
ENST00000679789.1:c.414+1G>T	ENSP00000506308.1:n.414+1G>T
ENST00000679826.1:c.-19+1G>T	ENSP00000505460.1:n.-19+1G>T
ENST00000681079.1:c.414+1G>T	ENSP00000506370.1:n.414+1G>T
ENST00000681237.1:c.*70+1G>T	ENSP00000505270.1:n.*70+1G>T
ENST00000681402.1:c.*124+1G>T	ENSP00000506692.1:n.*124+1G>T
ENST00000681766.1:c.414+1G>T	ENSP00000505161.1:n.414+1G>T
ENST00000409923.5:c.414+1G>T	ENSP00000386246.1:n.414+1G>T
ENST00000432176.6:c.414+1G>T	ENSP00000403396.2:n.414+1G>T
ENST00000440481.5:c.569+1G>T
ENST00000477349.5:n.504+1G>T
NM_032581.3:c.414+1G>T	NP_115970.2:n.414+1G>T
XM_005249894.3:c.414+1G>T	XP_005249951.1:n.414+1G>T
XM_005249895.1:c.414+1G>T	XP_005249952.1:n.414+1G>T
XM_006715799.2:c.5+1G>T	XP_006715862.1:n.5+1G>T
XM_011515589.1:c.414+1G>T	XP_011513891.1:n.414+1G>T
XM_011515590.1:c.414+1G>T	XP_011513892.1:n.414+1G>T
NM_001363466.1:c.414+1G>T	NP_001350395.1:n.414+1G>T
NM_001363467.1:c.414+1G>T	NP_001350396.1:n.414+1G>T
XM_011515589.2:c.414+1G>T	XP_011513891.1:n.414+1G>T
XM_011515590.2:c.414+1G>T	XP_011513892.1:n.414+1G>T
NM_001363466.2:c.414+1G>T	NP_001350395.1:n.414+1G>T
NM_001363467.2:c.414+1G>T	NP_001350396.1:n.414+1G>T
NM_032581.4:c.414+1G>T MANE Select	NP_115970.2:n.414+1G>T