Canonical Allele Identifier: CA726186047

Gene: MYOCD

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12714384A>T , CM000679.2:g.12714384A>T	GRCh38
NC_000017.10:g.12617701A>T , CM000679.1:g.12617701A>T	GRCh37
NC_000017.9:g.12558426A>T	NCBI36
NG_012972.1:g.53495A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000425538.6:c.122-1135A>T MANE Select	ENSP00000401678.1:n.122-1135A>T
ENST00000343344.8:c.122-1135A>T	ENSP00000341835.4:n.122-1135A>T
ENST00000425538.5:c.122-1135A>T	ENSP00000401678.1:n.122-1135A>T
ENST00000579237.5:c.*40-1135A>T	ENSP00000462694.1:n.*40-1135A>T
NM_001146312.2:c.122-1135A>T	NP_001139784.1:n.122-1135A>T
NM_153604.3:c.122-1135A>T	NP_705832.1:n.122-1135A>T
XM_005256863.1:c.122-1135A>T	XP_005256920.1:n.122-1135A>T
XM_005256864.1:c.-116-1135A>T	XP_005256921.1:n.-116-1135A>T
XM_017025342.1:c.122-1135A>T	XP_016880831.1:n.122-1135A>T
NM_001146312.3:c.122-1135A>T MANE Select	NP_001139784.1:n.122-1135A>T
NM_001378306.1:c.-116-1135A>T	NP_001365235.1:n.-116-1135A>T
NM_153604.4:c.122-1135A>T	NP_705832.1:n.122-1135A>T