Canonical Allele Identifier: CA365659049

Gene: MED23

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131591528C>A , CM000668.2:g.131591528C>A	GRCh38
NC_000006.11:g.131912668C>A , CM000668.1:g.131912668C>A	GRCh37
NC_000006.10:g.131954361C>A	NCBI36
NG_031860.1:g.41696G>T
NG_031860.2:g.41696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368068.8:c.3472-1G>T MANE Select	ENSP00000357047.3:n.3472-1G>T
ENST00000354577.8:c.3490-1G>T	ENSP00000346588.4:n.3490-1G>T
ENST00000368058.5:c.3490-1G>T	ENSP00000357037.1:n.3490-1G>T
ENST00000368060.7:c.3472-1G>T	ENSP00000357039.3:n.3472-1G>T
ENST00000368068.7:c.3472-1G>T	ENSP00000357047.3:n.3472-1G>T
ENST00000479213.1:n.1597-1G>T
ENST00000484885.1:n.457G>T
NM_001270521.1:c.3472-1G>T	NP_001257450.1:n.3472-1G>T
NM_001270522.1:c.3472-1G>T	NP_001257451.1:n.3472-1G>T
NM_004830.3:c.3472-1G>T	NP_004821.2:n.3472-1G>T
NM_015979.3:c.3490-1G>T	NP_057063.2:n.3490-1G>T
XM_005267223.1:c.3490-1G>T	XP_005267280.1:n.3490-1G>T
XM_011536257.1:c.3376-1G>T	XP_011534559.1:n.3376-1G>T
XM_005267223.3:c.3490-1G>T	XP_005267280.1:n.3490-1G>T
XM_011536257.3:c.3376-1G>T	XP_011534559.1:n.3376-1G>T
XM_017011501.1:c.2539-1G>T	XP_016866990.1:n.2539-1G>T
NM_004830.4:c.3472-1G>T MANE Select	NP_004821.2:n.3472-1G>T
NM_001270521.2:c.3472-1G>T	NP_001257450.1:n.3472-1G>T
NM_001270522.2:c.3472-1G>T	NP_001257451.1:n.3472-1G>T
NM_001376517.1:c.3490-1G>T	NP_001363446.1:n.3490-1G>T
NM_001376518.1:c.3418-1G>T	NP_001363447.1:n.3418-1G>T
NM_001376519.1:c.3334-1G>T	NP_001363448.1:n.3334-1G>T
NM_001376520.1:c.3331-1G>T	NP_001363449.1:n.3331-1G>T
NM_001376521.1:c.3334-1G>T	NP_001363450.1:n.3334-1G>T
NM_001376522.1:c.3301-1G>T	NP_001363451.1:n.3301-1G>T
NM_001376523.1:c.3217-1G>T	NP_001363452.1:n.3217-1G>T
NM_001376524.1:c.3085-1G>T	NP_001363453.1:n.3085-1G>T
NM_015979.4:c.3490-1G>T	NP_057063.2:n.3490-1G>T