Canonical Allele Identifier: CA2580075008

Gene: MED23

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131607924T>A , CM000668.2:g.131607924T>A	GRCh38
NC_000006.11:g.131929064T>A , CM000668.1:g.131929064T>A	GRCh37
NC_000006.10:g.131970757T>A	NCBI36
NG_031860.1:g.25300A>T
NG_031860.2:g.25300A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004830.4:c.1221+4A>T MANE Select	NP_004821.2:n.1221+4A>T
ENST00000368068.8:c.1221+4A>T MANE Select	ENSP00000357047.3:n.1221+4A>T
NM_001270521.1:c.1221+4A>T	NP_001257450.1:n.1221+4A>T
NM_001270521.2:c.1221+4A>T	NP_001257450.1:n.1221+4A>T
NM_001270522.1:c.1221+4A>T	NP_001257451.1:n.1221+4A>T
NM_001270522.2:c.1221+4A>T	NP_001257451.1:n.1221+4A>T
NM_001376517.1:c.1239+4A>T	NP_001363446.1:n.1239+4A>T
NM_001376518.1:c.1167+4A>T	NP_001363447.1:n.1167+4A>T
NM_001376519.1:c.1221+4A>T	NP_001363448.1:n.1221+4A>T
NM_001376520.1:c.1080+4A>T	NP_001363449.1:n.1080+4A>T
NM_001376521.1:c.1221+4A>T	NP_001363450.1:n.1221+4A>T
NM_001376522.1:c.1221+4A>T	NP_001363451.1:n.1221+4A>T
NM_001376523.1:c.966+4A>T	NP_001363452.1:n.966+4A>T
NM_001376524.1:c.1221+4A>T	NP_001363453.1:n.1221+4A>T
NM_004830.3:c.1221+4A>T	NP_004821.2:n.1221+4A>T
NM_015979.3:c.1239+4A>T	NP_057063.2:n.1239+4A>T
NM_015979.4:c.1239+4A>T	NP_057063.2:n.1239+4A>T
ENST00000354577.8:c.1239+4A>T	ENSP00000346588.4:n.1239+4A>T
ENST00000368053.8:c.1239+4A>T	ENSP00000357032.4:n.1239+4A>T
ENST00000368058.5:c.1239+4A>T	ENSP00000357037.1:n.1239+4A>T
ENST00000368060.7:c.1221+4A>T	ENSP00000357039.3:n.1221+4A>T
ENST00000368068.7:c.1221+4A>T	ENSP00000357047.3:n.1221+4A>T
ENST00000539158.1:c.1221+4A>T	ENSP00000445072.1:n.1221+4A>T
XM_005267223.1:c.1239+4A>T	XP_005267280.1:n.1239+4A>T
XM_005267223.3:c.1239+4A>T	XP_005267280.1:n.1239+4A>T
XM_006715612.2:c.1239+4A>T	XP_006715675.1:n.1239+4A>T
XM_006715612.3:c.1239+4A>T	XP_006715675.1:n.1239+4A>T
XM_011536257.1:c.1125+4A>T	XP_011534559.1:n.1125+4A>T
XM_011536257.3:c.1125+4A>T	XP_011534559.1:n.1125+4A>T
XM_017011501.1:c.288+4A>T	XP_016866990.1:n.288+4A>T