Canonical Allele Identifier: CA475792841

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77214690-C-T
• MyVariant Identifiers: chr11:g.76925735C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77214690C>T , CM000673.2:g.77214690C>T	GRCh38
NC_000011.9:g.76925735C>T , CM000673.1:g.76925735C>T	GRCh37
NC_000011.8:g.76603383C>T	NCBI36
NG_009086.1:g.91426C>T
NG_009086.2:g.91445C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6642C>T MANE Select	ENSP00000386331.3:p.Gly2214=
ENST00000670577.1:c.4443C>T
ENST00000409619.6:c.6495C>T	ENSP00000386635.2:p.Gly2165=
ENST00000409709.7:c.6642C>T	ENSP00000386331.3:p.Gly2214=
ENST00000458169.2:c.4068C>T	ENSP00000417017.2:p.Gly1356=
ENST00000458637.6:c.6522C>T	ENSP00000392185.2:p.Gly2174=
ENST00000481328.7:n.5192C>T
ENST00000605744.1:n.2156C>T
NM_000260.3:c.6642C>T	NP_000251.3:p.Gly2214=
NM_001127180.1:c.6522C>T	NP_001120652.1:p.Gly2174=
XM_005274012.2:c.6525C>T	XP_005274069.1:p.Gly2175=
XM_006718561.2:c.6528C>T	XP_006718624.1:p.Gly2176=
XR_949941.1:n.6936C>T
XM_017017780.1:c.6732C>T	XP_016873269.1:p.Gly2244=
XM_017017784.1:c.6615C>T	XP_016873273.1:p.Gly2205=
XM_017017788.1:c.6618C>T	XP_016873277.1:p.Gly2206=
XR_001747885.1:n.6721C>T
XR_001747887.1:n.6707C>T
NM_000260.4:c.6642C>T MANE Select	NP_000251.3:p.Gly2214=
NM_001127180.2:c.6522C>T	NP_001120652.1:p.Gly2174=
NM_001369365.1:c.6495C>T	NP_001356294.1:p.Gly2165=