Canonical Allele Identifier: CA346067100

Gene: POMC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25161464T>C , CM000664.2:g.25161464T>C	GRCh38
NC_000002.11:g.25384333T>C , CM000664.1:g.25384333T>C	GRCh37
NC_000002.10:g.25237837T>C	NCBI36
NG_008997.1:g.12227A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395826.7:c.421A>G MANE Select	ENSP00000379170.2:p.Met141Val
ENST00000264708.7:c.421A>G	ENSP00000264708.3:p.Met141Val
ENST00000380794.5:c.421A>G	ENSP00000370171.1:p.Met141Val
ENST00000395826.6:c.421A>G	ENSP00000379170.2:p.Met141Val
ENST00000405623.5:c.421A>G	ENSP00000384092.1:p.Met141Val
ENST00000449220.1:c.421A>G	ENSP00000387993.1:p.Met141Val
NM_000939.2:c.421A>G	NP_000930.1:p.Met141Val
NM_001035256.1:c.421A>G	NP_001030333.1:p.Met141Val
XM_011532917.1:c.421A>G	XP_011531219.1:p.Met141Val
NM_000939.3:c.421A>G	NP_000930.1:p.Met141Val
NM_001035256.2:c.421A>G	NP_001030333.1:p.Met141Val
NM_001319204.1:c.421A>G	NP_001306133.1:p.Met141Val
NM_001319205.1:c.421A>G	NP_001306134.1:p.Met141Val
NM_000939.4:c.421A>G MANE Select	NP_000930.1:p.Met141Val
NM_001319204.2:c.421A>G	NP_001306133.1:p.Met141Val
NM_001319205.2:c.421A>G	NP_001306134.1:p.Met141Val
NM_001035256.3:c.421A>G	NP_001030333.1:p.Met141Val