Canonical Allele Identifier: CA2405837795

Gene: MRTFA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.40600394A= , CM000684.2:g.40600394A=	GRCh38
NC_000022.10:g.40996398A= , CM000684.1:g.40996398A=	GRCh37
NC_000022.9:g.39326344A=	NCBI36
NG_065810.1:g.41326T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355630.10:c.-83-5659T= MANE Select	ENSP00000347847.5:n.-83-5659T=
ENST00000402042.7:c.-83-5659T=	ENSP00000385584.3:n.-83-5659T=
ENST00000463769.7:c.-22+36084T=	ENSP00000498788.2:n.-22+36084T=
ENST00000650658.1:n.172+36084T=
ENST00000651158.1:n.222-12816T=
ENST00000651595.2:c.-83-5659T=	ENSP00000498277.2:n.-83-5659T=
ENST00000355630.7:c.-383-5659T=	ENSP00000347847.3:n.-383-5659T=
ENST00000396617.7:c.-383-5659T=	ENSP00000379861.3:n.-383-5659T=
ENST00000402042.5:c.-383-5659T=	ENSP00000385584.1:n.-383-5659T=
ENST00000463769.6:n.210+36084T=
ENST00000466278.1:n.226-5659T=
NM_001282661.1:c.-383-5659T=	NP_001269590.1:n.-383-5659T=
NM_001282662.1:c.-383-5659T=	NP_001269591.1:n.-383-5659T=
NM_020831.4:c.-383-5659T=	NP_065882.1:n.-383-5659T=
XM_005261694.1:c.-322+36084T=	XP_005261751.1:n.-322+36084T=
XM_011530283.1:c.-451-5659T=	XP_011528585.1:n.-451-5659T=
XM_011530285.1:c.-566-5659T=	XP_011528587.1:n.-566-5659T=
XM_011530286.1:c.-978-5659T=	XP_011528588.1:n.-978-5659T=
NM_001282661.2:c.-83-5659T=	NP_001269590.2:n.-83-5659T=
NM_001282662.2:c.-83-5659T=	NP_001269591.2:n.-83-5659T=
NM_020831.5:c.-83-5659T=	NP_065882.2:n.-83-5659T=
XM_017028888.2:c.-390+36084T=	XP_016884377.1:n.-390+36084T=
NM_001282661.3:c.-83-5659T=	NP_001269590.2:n.-83-5659T=
NM_001282662.3:c.-83-5659T=	NP_001269591.2:n.-83-5659T=
NM_020831.6:c.-83-5659T= MANE Select	NP_065882.2:n.-83-5659T=