Canonical Allele Identifier: CA607771430

Gene: MED13L

Linked Data

• dbSNP Id: rs779461762
• gnomAD v2: 12-116675552-T-A
• gnomAD v3: 12-116237747-T-A
• gnomAD v4: 12-116237747-T-A
• MyVariant Identifiers: chr12:g.116675552T>A (hg19) ; chr12:g.116237747T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.116237747T>A , CM000674.2:g.116237747T>A	GRCh38
NC_000012.11:g.116675552T>A , CM000674.1:g.116675552T>A	GRCh37
NC_000012.10:g.115159935T>A	NCBI36
NG_023366.1:g.44440A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.73-42A>T MANE Select	ENSP00000281928.3:n.73-42A>T
ENST00000548743.2:c.43-42A>T	ENSP00000448553.2:n.43-42A>T
ENST00000551197.2:c.23-42A>T
ENST00000650226.1:c.73-42A>T	ENSP00000496981.1:n.73-42A>T
ENST00000650375.1:n.235-42A>T
ENST00000281928.7:c.73-42A>T	ENSP00000281928.3:n.73-42A>T
ENST00000548743.1:c.43-42A>T	ENSP00000448553.1:n.43-42A>T
ENST00000551197.1:n.23-42A>T
NM_015335.4:c.73-42A>T	NP_056150.1:n.73-42A>T
XM_011538080.1:c.73-42A>T	XP_011536382.1:n.73-42A>T
XM_011538081.1:c.73-42A>T	XP_011536383.1:n.73-42A>T
XM_011538082.1:c.43-42A>T	XP_011536384.1:n.43-42A>T
XM_011538080.2:c.73-42A>T	XP_011536382.1:n.73-42A>T
XM_011538081.2:c.73-42A>T	XP_011536383.1:n.73-42A>T
XM_011538082.2:c.43-42A>T	XP_011536384.1:n.43-42A>T
XM_017019090.1:c.73-42A>T	XP_016874579.1:n.73-42A>T
NM_015335.5:c.73-42A>T MANE Select	NP_056150.1:n.73-42A>T