Canonical Allele Identifier: CA386890755

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434958A>C (hg19) ; chr12:g.115997153A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997153A>C , CM000674.2:g.115997153A>C	GRCh38
NC_000012.11:g.116434958A>C , CM000674.1:g.116434958A>C	GRCh37
NC_000012.10:g.114919341A>C	NCBI36
NG_023366.1:g.285034T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2647T>G MANE Select	ENSP00000281928.3:p.Tyr883Asp
ENST00000548743.2:c.2617T>G	ENSP00000448553.2:p.Tyr873Asp
ENST00000549786.2:c.2075T>G
ENST00000647927.1:n.3020T>G
ENST00000648173.1:n.1442T>G
ENST00000648379.1:n.1015T>G
ENST00000648737.1:n.2411T>G
ENST00000648916.1:n.658T>G
ENST00000649607.1:c.831T>G
ENST00000650226.1:c.2647T>G	ENSP00000496981.1:p.Tyr883Asp
ENST00000281928.7:c.2647T>G	ENSP00000281928.3:p.Tyr883Asp
NM_015335.4:c.2647T>G	NP_056150.1:p.Tyr883Asp
XM_011538080.1:c.2647T>G	XP_011536382.1:p.Tyr883Asp
XM_011538081.1:c.2644T>G	XP_011536383.1:p.Tyr882Asp
XM_011538082.1:c.2617T>G	XP_011536384.1:p.Tyr873Asp
XM_011538080.2:c.2647T>G	XP_011536382.1:p.Tyr883Asp
XM_011538081.2:c.2644T>G	XP_011536383.1:p.Tyr882Asp
XM_011538082.2:c.2617T>G	XP_011536384.1:p.Tyr873Asp
XM_017019090.1:c.2644T>G	XP_016874579.1:p.Tyr882Asp
NM_015335.5:c.2647T>G MANE Select	NP_056150.1:p.Tyr883Asp