Canonical Allele Identifier: CA13153933

Gene: WDFY4 LRRC18

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48889774G>A , CM000672.2:g.48889774G>A	GRCh38
NC_000010.10:g.50097819G>A , CM000672.1:g.50097819G>A	GRCh37
NC_000010.9:g.49767825G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325239.12:c.7168-805G>A (WDFY4) MANE Select	ENSP00000320563.5:n.7168-805G>A
ENST00000325239.11:c.7168-805G>A (WDFY4)	ENSP00000320563.5:n.7168-805G>A
ENST00000265453.7:c.1428-805G>A (WDFY4)
ENST00000325239.9:c.7168-805G>A (WDFY4)	ENSP00000320563.5:n.7168-805G>A
NM_020945.1:c.7168-805G>A (WDFY4)	NP_065996.1:n.7168-805G>A
XM_005270004.2:c.7168-805G>A (WDFY4)	XP_005270061.1:n.7168-805G>A
XM_011539986.1:c.7168-805G>A (WDFY4)	XP_011538288.1:n.7168-805G>A
XM_011539987.1:c.7168-805G>A (WDFY4)	XP_011538289.1:n.7168-805G>A
XM_011539988.1:c.7168-805G>A (WDFY4)	XP_011538290.1:n.7168-805G>A
XR_945761.1:n.481-5434C>T (LRRC18)
XM_005270004.3:c.7168-805G>A (WDFY4)	XP_005270061.1:n.7168-805G>A
XM_011539986.3:c.7288-805G>A (WDFY4)	XP_011538288.2:n.7288-805G>A
XM_011539987.2:c.7288-805G>A (WDFY4)	XP_011538289.2:n.7288-805G>A
XM_011539988.2:c.7168-805G>A (WDFY4)	XP_011538290.1:n.7168-805G>A
XM_017016463.1:c.7168-805G>A (WDFY4)	XP_016871952.1:n.7168-805G>A
XM_017016464.1:c.3592-805G>A (WDFY4)	XP_016871953.1:n.3592-805G>A
XR_945761.2:n.481-5434C>T (LRRC18)
NM_020945.2:c.7168-805G>A (WDFY4)	NP_065996.1:n.7168-805G>A
NM_001394531.1:c.7168-805G>A (WDFY4) MANE Select	NP_001381460.1:n.7168-805G>A