Canonical Allele Identifier: CA2615262049

Gene: MYO7A

Linked Data

• gnomAD v4: 11-77211046-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.77211046G>C , CM000673.2:g.77211046G>C	GRCh38
NC_000011.9:g.76922091G>C , CM000673.1:g.76922091G>C	GRCh37
NC_000011.8:g.76599739G>C	NCBI36
NG_009086.1:g.87782G>C
NG_009086.2:g.87801G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409709.9:c.6052-106G>C MANE Select	ENSP00000386331.3:n.6052-106G>C
ENST00000670577.1:c.3853-106G>C
ENST00000409619.6:c.5905-106G>C	ENSP00000386635.2:n.5905-106G>C
ENST00000409709.7:c.6052-106G>C	ENSP00000386331.3:n.6052-106G>C
ENST00000458169.2:c.3478-106G>C	ENSP00000417017.2:n.3478-106G>C
ENST00000458637.6:c.5938-106G>C	ENSP00000392185.2:n.5938-106G>C
ENST00000481328.7:n.3588-106G>C
ENST00000526863.2:n.25+135G>C
ENST00000605744.1:n.1519-106G>C
NM_000260.3:c.6052-106G>C	NP_000251.3:n.6052-106G>C
NM_001127180.1:c.5938-106G>C	NP_001120652.1:n.5938-106G>C
XM_005274012.2:c.5935-106G>C	XP_005274069.1:n.5935-106G>C
XM_006718558.2:c.6043-106G>C	XP_006718621.1:n.6043-106G>C
XM_006718559.2:c.5938-106G>C	XP_006718622.1:n.5938-106G>C
XM_006718560.2:c.5935-106G>C	XP_006718623.1:n.5935-106G>C
XM_006718561.2:c.5938-106G>C	XP_006718624.1:n.5938-106G>C
XM_011545044.1:c.6052-106G>C	XP_011543346.1:n.6052-106G>C
XM_011545045.1:c.6046-106G>C	XP_011543347.1:n.6046-106G>C
XM_011545046.1:c.6019-106G>C	XP_011543348.1:n.6019-106G>C
XM_011545047.1:c.5956-106G>C	XP_011543349.1:n.5956-106G>C
XM_011545048.1:c.5827-106G>C	XP_011543350.1:n.5827-106G>C
XM_011545049.1:c.5815-106G>C	XP_011543351.1:n.5815-106G>C
XM_011545050.1:c.5788-106G>C	XP_011543352.1:n.5788-106G>C
XM_011545051.1:c.6052-106G>C	XP_011543353.1:n.6052-106G>C
XR_949938.1:n.6372-106G>C
XR_949941.1:n.6346-106G>C
XM_011545044.2:c.6052-106G>C	XP_011543346.1:n.6052-106G>C
XM_011545046.2:c.6142-106G>C	XP_011543348.2:n.6142-106G>C
XM_011545050.2:c.5788-106G>C	XP_011543352.1:n.5788-106G>C
XM_017017778.1:c.6136-106G>C	XP_016873267.1:n.6136-106G>C
XM_017017779.1:c.6133-106G>C	XP_016873268.1:n.6133-106G>C
XM_017017780.1:c.6142-106G>C	XP_016873269.1:n.6142-106G>C
XM_017017781.1:c.6046-106G>C	XP_016873270.1:n.6046-106G>C
XM_017017782.1:c.6028-106G>C	XP_016873271.1:n.6028-106G>C
XM_017017783.1:c.6025-106G>C	XP_016873272.1:n.6025-106G>C
XM_017017784.1:c.6025-106G>C	XP_016873273.1:n.6025-106G>C
XM_017017785.1:c.5905-106G>C	XP_016873274.1:n.5905-106G>C
XM_017017786.1:c.6142-106G>C	XP_016873275.1:n.6142-106G>C
XM_017017788.1:c.6028-106G>C	XP_016873277.1:n.6028-106G>C
XR_001747885.1:n.6131-106G>C
XR_001747886.1:n.6072-106G>C
XR_001747887.1:n.6117-106G>C
NM_000260.4:c.6052-106G>C MANE Select	NP_000251.3:n.6052-106G>C
NM_001127180.2:c.5938-106G>C	NP_001120652.1:n.5938-106G>C
NM_001369365.1:c.5905-106G>C	NP_001356294.1:n.5905-106G>C