Canonical Allele Identifier: CA386883641

Gene: MED13L

Linked Data

• MyVariant Identifiers: chr12:g.116422078C>A (hg19) ; chr12:g.115984273C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.115984273C>A , CM000674.2:g.115984273C>A	GRCh38
NC_000012.11:g.116422078C>A , CM000674.1:g.116422078C>A	GRCh37
NC_000012.10:g.114906461C>A	NCBI36
NG_023366.1:g.297914G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000281928.9:c.4438G>T MANE Select	ENSP00000281928.3:p.Val1480Leu
ENST00000549786.2:c.3866G>T
ENST00000648379.1:n.2806G>T
ENST00000648737.1:n.4202G>T
ENST00000648825.1:n.1178G>T
ENST00000648916.1:n.2449G>T
ENST00000649146.1:n.1168G>T
ENST00000649607.1:c.2622G>T
ENST00000649775.1:c.935G>T
ENST00000650091.1:n.2414G>T
ENST00000650226.1:c.4438G>T	ENSP00000496981.1:p.Val1480Leu
ENST00000281928.7:c.4438G>T	ENSP00000281928.3:p.Val1480Leu
NM_015335.4:c.4438G>T	NP_056150.1:p.Val1480Leu
XM_011538080.1:c.4438G>T	XP_011536382.1:p.Val1480Leu
XM_011538081.1:c.4435G>T	XP_011536383.1:p.Val1479Leu
XM_011538082.1:c.4408G>T	XP_011536384.1:p.Val1470Leu
XM_011538080.2:c.4438G>T	XP_011536382.1:p.Val1480Leu
XM_011538081.2:c.4435G>T	XP_011536383.1:p.Val1479Leu
XM_011538082.2:c.4408G>T	XP_011536384.1:p.Val1470Leu
XM_017019090.1:c.4435G>T	XP_016874579.1:p.Val1479Leu
NM_015335.5:c.4438G>T MANE Select	NP_056150.1:p.Val1480Leu