Canonical Allele Identifier: CA381935833

Gene: MYO7A

Linked Data

• MyVariant Identifiers: chr11:g.76922270A>C (hg19) ; chr11:g.77211225A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211225A>C , CM000673.2:g.77211225A>C	GRCh38
NC_000011.9:g.76922270A>C , CM000673.1:g.76922270A>C	GRCh37
NC_000011.8:g.76599918A>C	NCBI36
NG_009086.1:g.87961A>C
NG_009086.2:g.87980A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409709.9:c.6125A>C MANE Select	ENSP00000386331.3:p.Tyr2042Ser
ENST00000670577.1:c.3926A>C
ENST00000409619.6:c.5978A>C	ENSP00000386635.2:p.Tyr1993Ser
ENST00000409709.7:c.6125A>C	ENSP00000386331.3:p.Tyr2042Ser
ENST00000458169.2:c.3551A>C	ENSP00000417017.2:p.Tyr1184Ser
ENST00000458637.6:c.6011A>C	ENSP00000392185.2:p.Tyr2004Ser
ENST00000481328.7:n.3661A>C
ENST00000526863.2:n.25+314A>C
ENST00000605744.1:n.1592A>C
NM_000260.3:c.6125A>C	NP_000251.3:p.Tyr2042Ser
NM_001127180.1:c.6011A>C	NP_001120652.1:p.Tyr2004Ser
XM_005274012.2:c.6008A>C	XP_005274069.1:p.Tyr2003Ser
XM_006718558.2:c.6116A>C	XP_006718621.1:p.Tyr2039Ser
XM_006718559.2:c.6011A>C	XP_006718622.1:p.Tyr2004Ser
XM_006718560.2:c.6008A>C	XP_006718623.1:p.Tyr2003Ser
XM_006718561.2:c.6011A>C	XP_006718624.1:p.Tyr2004Ser
XM_011545044.1:c.6125A>C	XP_011543346.1:p.Tyr2042Ser
XM_011545045.1:c.6119A>C	XP_011543347.1:p.Tyr2040Ser
XM_011545046.1:c.6092A>C	XP_011543348.1:p.Tyr2031Ser
XM_011545047.1:c.6029A>C	XP_011543349.1:p.Tyr2010Ser
XM_011545048.1:c.5900A>C	XP_011543350.1:p.Tyr1967Ser
XM_011545049.1:c.5888A>C	XP_011543351.1:p.Tyr1963Ser
XM_011545050.1:c.5861A>C	XP_011543352.1:p.Tyr1954Ser
XM_011545051.1:c.6125A>C	XP_011543353.1:p.Tyr2042Ser
XR_949938.1:n.6445A>C
XR_949941.1:n.6419A>C
XM_011545044.2:c.6125A>C	XP_011543346.1:p.Tyr2042Ser
XM_011545046.2:c.6215A>C	XP_011543348.2:p.Tyr2072Ser
XM_011545050.2:c.5861A>C	XP_011543352.1:p.Tyr1954Ser
XM_017017778.1:c.6209A>C	XP_016873267.1:p.Tyr2070Ser
XM_017017779.1:c.6206A>C	XP_016873268.1:p.Tyr2069Ser
XM_017017780.1:c.6215A>C	XP_016873269.1:p.Tyr2072Ser
XM_017017781.1:c.6119A>C	XP_016873270.1:p.Tyr2040Ser
XM_017017782.1:c.6101A>C	XP_016873271.1:p.Tyr2034Ser
XM_017017783.1:c.6098A>C	XP_016873272.1:p.Tyr2033Ser
XM_017017784.1:c.6098A>C	XP_016873273.1:p.Tyr2033Ser
XM_017017785.1:c.5978A>C	XP_016873274.1:p.Tyr1993Ser
XM_017017786.1:c.6215A>C	XP_016873275.1:p.Tyr2072Ser
XM_017017788.1:c.6101A>C	XP_016873277.1:p.Tyr2034Ser
XR_001747885.1:n.6204A>C
XR_001747886.1:n.6145A>C
XR_001747887.1:n.6190A>C
NM_000260.4:c.6125A>C MANE Select	NP_000251.3:p.Tyr2042Ser
NM_001127180.2:c.6011A>C	NP_001120652.1:p.Tyr2004Ser
NM_001369365.1:c.5978A>C	NP_001356294.1:p.Tyr1993Ser