Canonical Allele Identifier: CA1908447730

Gene: WDFY4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48834906A>C , CM000672.2:g.48834906A>C	GRCh38
NC_000010.10:g.50042951A>C , CM000672.1:g.50042951A>C	GRCh37
NC_000010.9:g.49712957A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325239.12:c.6663+2197A>C MANE Select	ENSP00000320563.5:n.6663+2197A>C
ENST00000325239.11:c.6663+2197A>C	ENSP00000320563.5:n.6663+2197A>C
ENST00000265453.7:c.923+2197A>C
ENST00000325239.9:c.6663+2197A>C	ENSP00000320563.5:n.6663+2197A>C
NM_020945.1:c.6663+2197A>C	NP_065996.1:n.6663+2197A>C
XM_005270004.2:c.6663+2197A>C	XP_005270061.1:n.6663+2197A>C
XM_011539986.1:c.6663+2197A>C	XP_011538288.1:n.6663+2197A>C
XM_011539987.1:c.6663+2197A>C	XP_011538289.1:n.6663+2197A>C
XM_011539988.1:c.6663+2197A>C	XP_011538290.1:n.6663+2197A>C
XM_011539989.1:c.6783+2197A>C	XP_011538291.1:n.6783+2197A>C
XM_011539990.1:c.6783+2197A>C	XP_011538292.1:n.6783+2197A>C
XR_945951.1:n.633+196T>G
XR_945952.1:n.634-193T>G
XM_005270004.3:c.6663+2197A>C	XP_005270061.1:n.6663+2197A>C
XM_011539986.3:c.6783+2197A>C	XP_011538288.2:n.6783+2197A>C
XM_011539987.2:c.6783+2197A>C	XP_011538289.2:n.6783+2197A>C
XM_011539988.2:c.6663+2197A>C	XP_011538290.1:n.6663+2197A>C
XM_011539990.3:c.6783+2197A>C	XP_011538292.1:n.6783+2197A>C
XM_017016463.1:c.6663+2197A>C	XP_016871952.1:n.6663+2197A>C
XM_017016464.1:c.3087+2197A>C	XP_016871953.1:n.3087+2197A>C
XR_945951.2:n.4022+196T>G
XR_945952.2:n.4023-193T>G
NM_020945.2:c.6663+2197A>C	NP_065996.1:n.6663+2197A>C
NM_001394531.1:c.6663+2197A>C MANE Select	NP_001381460.1:n.6663+2197A>C