Canonical Allele Identifier: CA481949599

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116434980A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115997175A>G , CM000674.2:g.115997175A>G	GRCh38
NC_000012.11:g.116434980A>G , CM000674.1:g.116434980A>G	GRCh37
NC_000012.10:g.114919363A>G	NCBI36
NG_023366.1:g.285012T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.2625T>C MANE Select	ENSP00000281928.3:p.Pro875=
ENST00000548743.2:c.2595T>C	ENSP00000448553.2:p.Pro865=
ENST00000549786.2:c.2053T>C
ENST00000647927.1:n.2998T>C
ENST00000648173.1:n.1420T>C
ENST00000648379.1:n.993T>C
ENST00000648737.1:n.2389T>C
ENST00000648916.1:n.636T>C
ENST00000649607.1:c.809T>C
ENST00000650226.1:c.2625T>C	ENSP00000496981.1:p.Pro875=
ENST00000281928.7:c.2625T>C	ENSP00000281928.3:p.Pro875=
NM_015335.4:c.2625T>C	NP_056150.1:p.Pro875=
XM_011538080.1:c.2625T>C	XP_011536382.1:p.Pro875=
XM_011538081.1:c.2622T>C	XP_011536383.1:p.Pro874=
XM_011538082.1:c.2595T>C	XP_011536384.1:p.Pro865=
XM_011538080.2:c.2625T>C	XP_011536382.1:p.Pro875=
XM_011538081.2:c.2622T>C	XP_011536383.1:p.Pro874=
XM_011538082.2:c.2595T>C	XP_011536384.1:p.Pro865=
XM_017019090.1:c.2622T>C	XP_016874579.1:p.Pro874=
NM_015335.5:c.2625T>C MANE Select	NP_056150.1:p.Pro875=