Canonical Allele Identifier: CA481948788

Gene: MED13L

Linked Data

• gnomAD v4: 12-115991804-T-A
• MyVariant Identifiers: chr12:g.116429609T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115991804T>A , CM000674.2:g.115991804T>A	GRCh38
NC_000012.11:g.116429609T>A , CM000674.1:g.116429609T>A	GRCh37
NC_000012.10:g.114913992T>A	NCBI36
NG_023366.1:g.290383A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281928.9:c.3150A>T MANE Select	ENSP00000281928.3:p.Thr1050=
ENST00000548743.2:c.3120A>T	ENSP00000448553.2:p.Thr1040=
ENST00000549786.2:c.2578A>T
ENST00000648173.1:n.1945A>T
ENST00000648379.1:n.1518A>T
ENST00000648737.1:n.2914A>T
ENST00000648916.1:n.1161A>T
ENST00000649607.1:c.1334A>T
ENST00000650226.1:c.3150A>T	ENSP00000496981.1:p.Thr1050=
ENST00000281928.7:c.3150A>T	ENSP00000281928.3:p.Thr1050=
NM_015335.4:c.3150A>T	NP_056150.1:p.Thr1050=
XM_011538080.1:c.3150A>T	XP_011536382.1:p.Thr1050=
XM_011538081.1:c.3147A>T	XP_011536383.1:p.Thr1049=
XM_011538082.1:c.3120A>T	XP_011536384.1:p.Thr1040=
XM_011538080.2:c.3150A>T	XP_011536382.1:p.Thr1050=
XM_011538081.2:c.3147A>T	XP_011536383.1:p.Thr1049=
XM_011538082.2:c.3120A>T	XP_011536384.1:p.Thr1040=
XM_017019090.1:c.3147A>T	XP_016874579.1:p.Thr1049=
NM_015335.5:c.3150A>T MANE Select	NP_056150.1:p.Thr1050=