Canonical Allele Identifier: CA386889179

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116429759G>T (hg19) ; chr12:g.115991954G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991954G>T , CM000674.2:g.115991954G>T	GRCh38
NC_000012.11:g.116429759G>T , CM000674.1:g.116429759G>T	GRCh37
NC_000012.10:g.114914142G>T	NCBI36
NG_023366.1:g.290233C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3000C>A MANE Select	ENSP00000281928.3:p.Asn1000Lys
ENST00000548743.2:c.2970C>A	ENSP00000448553.2:p.Asn990Lys
ENST00000549786.2:c.2428C>A
ENST00000648173.1:n.1795C>A
ENST00000648379.1:n.1368C>A
ENST00000648737.1:n.2764C>A
ENST00000648916.1:n.1011C>A
ENST00000649607.1:c.1184C>A
ENST00000650226.1:c.3000C>A	ENSP00000496981.1:p.Asn1000Lys
ENST00000281928.7:c.3000C>A	ENSP00000281928.3:p.Asn1000Lys
NM_015335.4:c.3000C>A	NP_056150.1:p.Asn1000Lys
XM_011538080.1:c.3000C>A	XP_011536382.1:p.Asn1000Lys
XM_011538081.1:c.2997C>A	XP_011536383.1:p.Asn999Lys
XM_011538082.1:c.2970C>A	XP_011536384.1:p.Asn990Lys
XM_011538080.2:c.3000C>A	XP_011536382.1:p.Asn1000Lys
XM_011538081.2:c.2997C>A	XP_011536383.1:p.Asn999Lys
XM_011538082.2:c.2970C>A	XP_011536384.1:p.Asn990Lys
XM_017019090.1:c.2997C>A	XP_016874579.1:p.Asn999Lys
NM_015335.5:c.3000C>A MANE Select	NP_056150.1:p.Asn1000Lys