Canonical Allele Identifier: CA881531741

Gene: ANKRD27 NUDT19

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.32672197A>T , CM000681.2:g.32672197A>T	GRCh38
NC_000019.9:g.33163103A>T , CM000681.1:g.33163103A>T	GRCh37
NC_000019.8:g.37854943A>T	NCBI36
NG_016751.1:g.1791A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000306065.9:c.-31+2874T>A (ANKRD27) MANE Select	ENSP00000304292.3:n.-31+2874T>A
ENST00000306065.8:c.-31+2874T>A (ANKRD27)	ENSP00000304292.3:n.-31+2874T>A
ENST00000586463.5:c.-535+2874T>A (ANKRD27)	ENSP00000467447.1:n.-535+2874T>A
ENST00000586693.7:c.-31+2874T>A (ANKRD27)	ENSP00000476897.1:n.-31+2874T>A
ENST00000587352.5:c.-31+2874T>A (ANKRD27)	ENSP00000466138.1:n.-31+2874T>A
ENST00000588700.5:c.-31+2874T>A (ANKRD27)	ENSP00000466905.1:n.-31+2874T>A
ENST00000590519.2:c.-31+3589T>A (ANKRD27)	ENSP00000464819.1:n.-31+3589T>A
ENST00000622502.4:c.-31+2874T>A (ANKRD27)	ENSP00000480730.1:n.-31+2874T>A
NM_032139.2:c.-31+2874T>A (ANKRD27)	NP_115515.2:n.-31+2874T>A
XM_005258925.3:c.-24-1061A>T (NUDT19)	XP_005258982.1:n.-24-1061A>T
XM_006723412.2:c.-31+2697T>A (ANKRD27)	XP_006723475.1:n.-31+2697T>A
XM_017027349.1:c.-462+2874T>A (ANKRD27)	XP_016882838.1:n.-462+2874T>A
NM_032139.3:c.-31+2874T>A (ANKRD27) MANE Select	NP_115515.2:n.-31+2874T>A