Canonical Allele Identifier: CA2123464853

Gene: MYH7 MHRT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23415919_23415920delinsTA , CM000676.2:g.23415919_23415920delinsTA	GRCh38
NC_000014.8:g.23885128_23885129delinsTA , CM000676.1:g.23885128_23885129delinsTA	GRCh37
NC_000014.7:g.22954968_22954969delinsTA	NCBI36
NG_007884.1:g.24742_24743delinsTA , LRG_384:g.24742_24743delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4953+84_4953+85delinsTA (MYH7) MANE Select	ENSP00000347507.3:n.4953+84_4953+85delinsTA
ENST00000355349.3:c.4953+84_4953+85delinsTA (MYH7)	ENSP00000347507.3:n.4953+84_4953+85delinsTA
NM_000257.3:c.4953+84_4953+85delinsTA (MYH7)	NP_000248.2:n.4953+84_4953+85delinsTA
NR_126491.1:n.262-82_262-81delinsTA (MHRT)
XM_017021340.1:c.4953+84_4953+85delinsTA (MYH7)	XP_016876829.1:n.4953+84_4953+85delinsTA
NM_000257.4:c.4953+84_4953+85delinsTA (MYH7) MANE Select	NP_000248.2:n.4953+84_4953+85delinsTA