Canonical Allele Identifier: CA1008868873

Gene: MPC2

Linked Data

• gnomAD v3: 1-167933825-T-TTA
• gnomAD v4: 1-167933825-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.167933825_167933826insTA , CM000663.2:g.167933825_167933826insTA	GRCh38
NC_000001.10:g.167903063_167903064insTA , CM000663.1:g.167903063_167903064insTA	GRCh37
NC_000001.9:g.166169687_166169688insTA	NCBI36
NG_053062.1:g.2587_2588insTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000271373.9:c.109+1907_109+1908insTA MANE Select	ENSP00000271373.4:n.109+1907_109+1908insTA
ENST00000271373.8:c.109+1907_109+1908insTA	ENSP00000271373.4:n.109+1907_109+1908insTA
ENST00000367846.8:c.109+1907_109+1908insTA	ENSP00000356820.4:n.109+1907_109+1908insTA
ENST00000458574.1:c.109+1907_109+1908insTA	ENSP00000392874.1:n.109+1907_109+1908insTA
NM_001143674.3:c.109+1907_109+1908insTA	NP_001137146.1:n.109+1907_109+1908insTA
NM_015415.3:c.109+1907_109+1908insTA	NP_056230.1:n.109+1907_109+1908insTA
NR_026550.2:n.469+1907_469+1908insTA
XM_006711266.2:c.109+1907_109+1908insTA	XP_006711329.1:n.109+1907_109+1908insTA
XM_006711266.3:c.109+1907_109+1908insTA	XP_006711329.1:n.109+1907_109+1908insTA
NM_001143674.4:c.109+1907_109+1908insTA MANE Select	NP_001137146.1:n.109+1907_109+1908insTA
NR_026550.3:n.264+1907_264+1908insTA