Canonical Allele Identifier: CA365664888

Gene: MED23

Linked Data - Expert Curation

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131596164C>G , CM000668.2:g.131596164C>G	GRCh38
NC_000006.11:g.131917304C>G , CM000668.1:g.131917304C>G	GRCh37
NC_000006.10:g.131958997C>G	NCBI36
NG_031860.1:g.37060G>C
NG_031860.2:g.37060G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368068.8:c.2779-1G>C MANE Select	ENSP00000357047.3:n.2779-1G>C
ENST00000354577.8:c.2797-1G>C	ENSP00000346588.4:n.2797-1G>C
ENST00000368058.5:c.2797-1G>C	ENSP00000357037.1:n.2797-1G>C
ENST00000368060.7:c.2779-1G>C	ENSP00000357039.3:n.2779-1G>C
ENST00000368068.7:c.2779-1G>C	ENSP00000357047.3:n.2779-1G>C
ENST00000479213.1:n.358G>C
NM_001270521.1:c.2779-1G>C	NP_001257450.1:n.2779-1G>C
NM_001270522.1:c.2779-1G>C	NP_001257451.1:n.2779-1G>C
NM_004830.3:c.2779-1G>C	NP_004821.2:n.2779-1G>C
NM_015979.3:c.2797-1G>C	NP_057063.2:n.2797-1G>C
XM_005267223.1:c.2797-1G>C	XP_005267280.1:n.2797-1G>C
XM_011536257.1:c.2683-1G>C	XP_011534559.1:n.2683-1G>C
XM_005267223.3:c.2797-1G>C	XP_005267280.1:n.2797-1G>C
XM_011536257.3:c.2683-1G>C	XP_011534559.1:n.2683-1G>C
XM_017011501.1:c.1846-1G>C	XP_016866990.1:n.1846-1G>C
NM_004830.4:c.2779-1G>C MANE Select	NP_004821.2:n.2779-1G>C
NM_001270521.2:c.2779-1G>C	NP_001257450.1:n.2779-1G>C
NM_001270522.2:c.2779-1G>C	NP_001257451.1:n.2779-1G>C
NM_001376517.1:c.2797-1G>C	NP_001363446.1:n.2797-1G>C
NM_001376518.1:c.2725-1G>C	NP_001363447.1:n.2725-1G>C
NM_001376519.1:c.2641-1G>C	NP_001363448.1:n.2641-1G>C
NM_001376520.1:c.2638-1G>C	NP_001363449.1:n.2638-1G>C
NM_001376521.1:c.2641-1G>C	NP_001363450.1:n.2641-1G>C
NM_001376522.1:c.2608-1G>C	NP_001363451.1:n.2608-1G>C
NM_001376523.1:c.2524-1G>C	NP_001363452.1:n.2524-1G>C
NM_001376524.1:c.2392-1G>C	NP_001363453.1:n.2392-1G>C
NM_015979.4:c.2797-1G>C	NP_057063.2:n.2797-1G>C