Canonical Allele Identifier: CA10683064

Gene: MYBPHL

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109297274C>T , CM000663.2:g.109297274C>T	GRCh38
NC_000001.10:g.109839896C>T , CM000663.1:g.109839896C>T	GRCh37
NC_000001.9:g.109641419C>T	NCBI36
NG_032757.1:g.14768G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357155.2:c.431-85G>A MANE Select	ENSP00000349678.1:n.431-85G>A
ENST00000357155.1:c.431-85G>A	ENSP00000349678.1:n.431-85G>A
ENST00000477962.1:n.150-1977G>A
NM_001010985.2:c.431-85G>A	NP_001010985.2:n.431-85G>A
NM_001265613.1:c.362-85G>A	NP_001252542.1:n.362-85G>A
XM_017001173.1:c.431-85G>A	XP_016856662.1:n.431-85G>A
XM_017001174.1:c.431-85G>A	XP_016856663.1:n.431-85G>A
XM_017001175.1:c.362-85G>A	XP_016856664.1:n.362-85G>A
NM_001010985.3:c.431-85G>A MANE Select	NP_001010985.2:n.431-85G>A
NM_001265613.2:c.362-85G>A	NP_001252542.1:n.362-85G>A